Search Result
Results for "
tert-butyl-4-
" in MedChemExpress (MCE) Product Catalog:
2
Biochemical Assay Reagents
12
Isotope-Labeled Compounds
| Cat. No. |
Product Name |
Target |
Research Areas |
Chemical Structure |
-
- HY-69260
-
|
|
PROTAC Linkers
|
Others
|
|
tert-Butyl 4-formylpiperidine-1-carboxylate is a PROTAC linker and can be used in the synthesis of PROTAC BRM/BRG1 degrader-3 (HY-168251) .
|
-
-
- HY-W012339
-
|
N-Boc-putrescine
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-aminobutyl)carbamate hydrochloride (N-Boc-putrescine) is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-34415
-
|
tert-butyl 4-Bromobutyrate
|
PROTAC Linkers
|
Cancer
|
|
4-Bromobutanoic acid tert-butyl ester (tert-Butyl 4-Bromobutyrate) is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W091986
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperidin-4-ylmethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W077402
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-bromopropyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-60172
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4,7-diazaspiro[2.5]octane-7-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
-
- HY-W018070
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(bromomethyl)benzylcarbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W442050
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(methylamino)butanoate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W045082
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperidine-4-carbonyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W033724
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperidin-4-yl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W074901
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperazin-1-ylmethyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W076878
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(prop-2-yn-1-yl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-33021
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-hydroxybutyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-32208
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
-
- HY-W019095
-
-
-
- HY-W046402
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(hydroxymethyl)benzylcarbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W101721
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-chlorobutyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W071973
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperazin-1-yl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W087467
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(prop-2-yn-1-yl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-33846
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W005822
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-bromoethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W001613
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-cyanoacetyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W015220
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-hydroxybutyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W011657
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(bromomethyl)benzoate is a synthetic intermediate useful for compound synthesis .
|
-
-
- HY-W042233
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-hydroxycyclohexyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W093332
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-amino-3-fluorobenzoate is a drug intermediate for synthesis of various active compounds.
|
-
-
- HY-W001461
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(((methylsulfonyl)oxy)methyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-78698
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl (4-(prop-2-yn-1-yloxy)benzyl)carbamate is a drug intermediate for synthesis of various active compounds.
|
-
-
- HY-22289
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-aminobicyclo[2.2.2]octan-1-yl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-42363
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4,4,4-trifluorobut-2-enoate is a drug intermediate for synthesis of various active compounds.
|
-
-
- HY-W012020
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-hydroxypropyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W129547
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-bromopropyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W046163
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-aminopropyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W102095
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W054209
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-hydroxyprop-1-yn-1-yl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-40180
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(methylamino)butylcarbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W024496
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl ((4-oxocyclohexyl)methyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-40179
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-aminobutyl)(methyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W892600
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-(aminooxy)butyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W803700
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl (4-(aminomethyl)benzyl)(methyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W003177
-
|
|
Biochemical Assay Reagents
|
Others
|
|
tert-Butyl 4-iodopiperidine-1-carboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
-
- HY-21376S
-
-
-
- HY-W042263
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(aminomethyl)-4-fluoropiperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W087218
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperidin-3-ylmethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-20669
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(azetidin-3-yl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W056396
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(azetidin-3-yl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W456646
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(hydroxymethyl)-5-methoxy-7-methyl-1H-indole-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
-
- HY-W176791
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(3-chloropropyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W241239
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-hydroxyethoxy)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
-
- HY-W003678
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-bromophenyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W090887
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-bromophenoxy)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W039512
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-cyanophenyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W004998
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-chloroethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W274524
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(4-(hydroxymethyl)benzyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W003950
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-(methylamino)ethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-76929S
-
-
- HY-77169
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-ethoxy-2-oxoethyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W141391
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-((methylsulfonyl)oxy)ethyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-20880
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-hydroxypropyl)tetrahydropyridine-1(2H)-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-I0122
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(2-carbamoylbenzofuran-5-yl)piperazine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-W001731
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-Aminoethyl)-3,3-difluoropiperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W615225
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-oxobutanoate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W069230
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-chlorobutanoate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W740068
-
-
- HY-W089549
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl(4-iodobutoxy)dimethylsilane is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W700253
-
|
|
Isotope-Labeled Compounds
|
Others
|
|
tert-Butyl 4-methylpiperazine-1-carboxylate-d8 is the deuterium labeled tert-Butyl 4-methylpiperazine-1-carboxylate (HY-W050208).
|
-
- HY-W096540
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-bromobenzyl)(methyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W160464
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-cyanopiperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W046507
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(cyanomethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W088455
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-(piperazin-1-yl)butyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W056397
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(azetidin-3-yl)piperazine-1-carboxylate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W034462
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-aminobut-2-en-1-yl)carbamate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W293739
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(hydroxymethyl)-[1,4'-bipiperidine]-1'-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W056046
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-hydroxybicyclo[2.2.2]octan-1-yl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W043300
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-aminopropyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W125143
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-aminophenyl)piperazine-1-carboxylate hydrochloride is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W046489
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(2-bromoethyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W353239
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(2-chloroacetyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W024432
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-(hydroxymethyl)phenyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W006350
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-(methylamino)ethyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W069337
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-((2-hydroxyethoxy)methyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W102038
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-aminoethyl)-3-oxopiperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-169975
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-(piperazin-1-ylmethyl)piperidin-1-yl)benzoate is a PROTAC linker. tert-Butyl 4-(4-(piperazin-1-ylmethyl)piperidin-1-yl)benzoate can be used to synthesize PROTAC AR Degrader-6 (HY-156751) .
|
-
- HY-32208S
-
|
|
Isotope-Labeled Compounds
|
Others
|
|
tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate-d4 is the deuterium labeled tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate[1].
|
-
- HY-W009359S
-
-
- HY-W704049
-
|
|
Isotope-Labeled Compounds
|
Others
|
|
tert-Butyl 4-(methyl-d3)piperazine-1-carboxylate is the deuterium labeled tert-Butyl 4-methylpiperazine-1-carboxylate (HY-W050208).
|
-
- HY-W424224
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl (4-(hydroxymethyl)benzyl)(methyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W353135
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl (4-((tert-butoxycarbonyl)amino)phenethyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W349542
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(piperazine-1-carbonyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W092078
-
|
|
Biochemical Assay Reagents
|
Others
|
|
tert-Butyl (4-iodobutyl)carbamate is a four carbon linker containing a Boc-protected amino group and an iodine group. The Boc group can be deprotected under mild acidic conditions to form the free amine. Iodine (I) is a very good leaving group for nucleophilic substitution reactions.
|
-
- HY-W380469
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperazin-1-yl)piperidine-1-carboxylate (dihydrochloride) is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W377732
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(piperidin-3-ylmethyl)piperazine-1-carboxylate (dihydrochloride) is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W099109
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-(ethoxycarbonyl)phenoxy)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W107433
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-(hydroxymethyl)phenoxy)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W109687
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(3-bromopropyl)piperazine-1-carboxylate oxalate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W424242
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(4-(aminomethyl)benzyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W145021
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-(aminomethyl)benzoyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W674400
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-(2-prop-2-ynoxyethyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-120021
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylate is a synthetic intermediate useful for pharmaceutical synthesis..
|
-
- HY-W380868
-
|
|
PROTAC Linkers
|
Cancer
|
|
Tert-butyl 4-((1r,4r)-4-aminocyclohexyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W244439
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(2-ethoxy-1,1-difluoro-2-oxoethyl)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-43553
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl (4-((5-fluoro-7-(2-methoxyethoxy)quinazolin-4-yl)amino)phenyl)carbamate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-79039
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-[[2-(4-chlorophenyl)-4,4-dimethylcyclohex-1-enyl]methyl]piperazine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-77600
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(3-methyl-1-phenyl-1H-pyrazol-5-yl)piperazine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-W095444
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenethyl)carbamate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W001761
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-butyl 4-(2-Ethoxy-1,1-difluoro-2-oxoethyl)-5,6-dihydropyridine-1(2H)-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W059361
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)piperidine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-23483
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl (4-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)butyl)carbamate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-W094102
-
|
|
PROTAC Linkers
|
Cancer
|
|
tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoyl)piperazine-1-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
|
-
- HY-W580291
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl (4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5-((triisopropylsilyl)ethynyl)naphthalen-2-yl)carbamate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-75951
-
|
|
Drug Intermediate
|
Others
|
|
tert-Butyl 4-(6-(8-cyclopentyl-5-Methyl-7-oxo-6-(1-propoxyvinyl)-7,8-dihydropyrido[2,3-d]pyriMidin-2-ylaMino)pyridin-3-yl)piperazine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-W010037
-
|
|
Environmental Pollutants
COX
|
Inflammation/Immunology
|
|
2-tert-Butyl-4-methoxyphenol is a major component of Butylhydroxyanisole (BHA) (HY-B1066). 2-tert-Butyl-4-methoxyphenol is an antioxidant agent, that inhibits expression of Cox2 and Tnfa genes upon stimulation with Lipopolysaccharides (HY-D1056). 2-tert-Butyl-4-methoxyphenol exhibits anti-inflammatory activity, combined with 2,6-di-tert-butyl-4-methylphenol (BHT) .
|
-
- HY-W010037R
-
|
|
Reference Standards
COX
|
Inflammation/Immunology
|
|
2-(tert-Butyl)-4-methoxyphenol (Standard) is the analytical standard of 2-(tert-Butyl)-4-methoxyphenol. This product is intended for research and analytical applications. 2-tert-Butyl-4-methoxyphenol is a major component of Butylhydroxyanisole (BHA) (HY-B1066). 2-tert-Butyl-4-methoxyphenol is an antioxidant agent, that inhibits expression of Cox2 and Tnfa genes upon stimulation with Lipopolysaccharides (HY-D1056). 2-tert-Butyl-4-methoxyphenol exhibits anti-inflammatory activity, combined with 2,6-di-tert-butyl-4-methylphenol (BHT) .
|
-
- HY-W010037S
-
-
- HY-W024365S
-
-
- HY-W024365R
-
|
|
PROTAC Linkers
Reference Standards
|
Cancer
|
|
3-tert-Butyl-4-methoxyphenol (Standard) is the analytical standard of 3-tert-Butyl-4-methoxyphenol. This product is intended for research and analytical applications. 3-tert-Butyl-4-methoxyphenol is a PROTAC linker, belongs to alkyl/ether class, with insecticidal activity. 3-tert-Butyl-4-methoxyphenol also induced increased activities of glutathione (GSH) S-transferase and epoxide hydrolase in the liver and forestomach tissues of A/HeJ mice, regulating the carcinogen metabolism system .
|
-
- HY-W102287R
-
|
|
Reference Standards
|
|
|
3,5-Di-tert-butyl-4-hydroxybenzoic acid (Standard) is the analytical standard of 3,5-Di-tert-butyl-4-hydroxybenzoic acid. This product is intended for research and analytical applications.
|
-
- HY-W024365
-
|
|
PROTAC Linkers
|
Cancer
|
|
3-tert-Butyl-4-methoxyphenol is a PROTAC linker, belongs to alkyl/ether class, with insecticidal activity. 3-tert-Butyl-4-methoxyphenol also induced increased activities of glutathione (GSH) S-transferase and epoxide hydrolase in the liver and forestomach tissues of A/HeJ mice, regulating the carcinogen metabolism system .
|
-
- HY-W099555R
-
|
Stearyl 3-(3,5-Di-tert-butyl-4-hydroxyphenyl)propionate (Standard)
|
Reference Standards
|
|
|
Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate (Standard) is the analytical standard of Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate. This product is intended for research and analytical applications.
|
-
- HY-W012187R
-
|
BHT-CHO (Standard)
|
Reference Standards
Drug Metabolite
|
Cancer
|
|
3,5-Di-tert-butyl-4-hydroxybenzaldehyde (Standard) is the analytical standard of 3,5-Di-tert-butyl-4-hydroxybenzaldehyde. This product is intended for research and analytical applications. 3,5-Di-tert-butyl-4-hydroxybenzaldehyde (BHT-CHO) is a metabolite of Butylated hydroxytoluene (HY-Y0172) .
|
-
- HY-W283336S
-
-
- HY-W077436S
-
-
- HY-W007500
-
|
|
Biochemical Assay Reagents
|
Others
|
|
2,6-Di-Tert-butyl-4-methylpyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W012187
-
|
BHT-CHO
|
Drug Metabolite
|
Cancer
|
|
3,5-Di-tert-butyl-4-hydroxybenzaldehyde (BHT-CHO) is a metabolite of Butylated hydroxytoluene (HY-Y0172) .
|
-
- HY-W267318R
-
|
|
Reference Standards
|
|
|
1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethan-1-one (Standard) is the analytical standard of 1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethan-1-one. This product is intended for research and analytical applications.
|
-
- HY-W890392
-
|
|
PROTAC Linkers
|
Cancer
|
|
(1r,4r)-tert-Butyl 4-(bromomethyl)cyclohexanecarboxylate is a PROTAC linker used in the synthesis of SMD-1087 (HY-170828) .
|
-
- HY-173163
-
|
|
Bacterial
|
Infection
|
|
(E)-2,6-Di-tert-butyl-4-(4-(diethylamino)styryl)pyrylium (trifluoromethanesulfonate) (Compound 4a) is a Gram-negative outer membrane permeabilizer with synergistic antibacterial activity through the blockage on LptA/LptC interaction via targeting Met47 in LptA. (E)-2,6-Di-tert-butyl-4-(4-(diethylamino)styryl)pyrylium (trifluoromethanesulfonate) potentiates pol B against both wild-typed and MDR A. baumannii and E. coli strains. (E)-2,6-Di-tert-butyl-4-(4-(diethylamino)styryl)pyrylium (trifluoromethanesulfonate) can be used as antibiotic adjuvants against MDR Gram-negative bacteria .
|
-
- HY-W643129
-
|
|
Drug Derivative
|
Others
|
|
1-(3,5-Di-tert-butyl-4-hydroxyphenyl)ethane-1,2-diol is a sterically hindered para-alkylphenol.
|
-
- HY-W010677R
-
|
Tris-(3,5-di-tert-butyl-4-hydroxybenzyl)-isocyanurate (Standard)
|
Reference Standards
|
|
|
1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-1,3,5-triazinane-2,4,6-trione (Standard) is the analytical standard of 1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-1,3,5-triazinane-2,4,6-trione. This product is intended for research and analytical applications.
|
-
- HY-W077436S1
-
|
2,6-Di-tert-butyl-4-Methoxyphenol-d18
|
Isotope-Labeled Compounds
|
Others
|
|
Butylated hydroxyanisole-d18 (2,6-Di-Tert-Butyl-4-Methoxyphenol-d18) is the deuterium labeled Butylated hydroxyanisole.
|
-
- HY-W094776
-
|
2,7-Di-tert-butyl-4,5-pyrenediketone
|
MOFs
|
Others
|
|
2,7-Di-tert-butylpyrene-4,5-dione (2,7-Di-tert-butyl-4,5-pyrenediketone) is a metal-organic framework (MOF).
|
-
- HY-W456508
-
|
|
MOFs
|
Others
|
|
2',5'-Di-tert-butyl-4,4''-dihydroxy-[1,1':4',1''-terphenyl]-3,3''-dicarboxylic acid is a metal-organic framework (MOF).
|
-
- HY-W075323
-
|
|
MOFs
|
Others
|
|
4,4'-(2,8-Di-tert-butyl-4,10-dihydropyreno[4,5-d:9,10-d']diimidazole-5,11-diyl)dibenzoic acid is a metal-organic framework (MOF).
|
-
- HY-W042234R
-
|
tert-butyl(3R,5S)-6-oxo-3,5-O-iso-propylidene-3,5-dihydroxyhexanoate (Standard)
|
Reference Standards
|
|
|
tert-Butyl [(4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl]acetate (Standard) is the analytical standard of tert-Butyl [(4R,6S)-6-formyl-2,2-dimethyl-1,3-dioxan-4-yl]acetate (HY-W042234). This product is intended for research and analytical applications.
|
-
- HY-W076424R
-
|
|
Reference Standards
|
|
|
tert-Butyl (4R,5R)-4-(hydroxymethyl)-2,2-dimethyl-5-phenyloxazolidine-3-carboxylate (Standard) is the analytical standard of tert-Butyl (4R,5R)-4-(hydroxymethyl)-2,2-dimethyl-5-phenyloxazolidine-3-carboxylate. This product is intended for research and analytical applications.
|
-
- HY-W040301
-
-
- HY-103502
-
CGP7930
1 Publications Verification
|
GABA Receptor
|
Neurological Disease
|
|
CGP7930 (3-(3’,5’-Di-tert-butyl-4’-hydroxy) phenyl-2, 2-dimethylpropanol) is a positive metabotropic GABAB receptor allosteric modulator. CGP7930 enhances the inhibitory effect of l-baclofen on the oscillatory activity of cultured cortical neurons .
|
-
- HY-W017330
-
|
|
Biochemical Assay Reagents
|
Others
|
|
Methacrylic anhydride is a typical polymerizable 1,6-diolefin. Methacrylic anhydride can form a soluble csyclopolymer by free-radical initiation. Methacrylic anhydride can spontaneously polymerize through the vinyl group and justifies the use of 2-6-di-tert-butyl4-methylphenol as an inhibitor .
|
-
- HY-135617R
-
|
N,N'-Hexane-1,6-diylbis[3,5-di-tert-butyl-4-hydroxyphenylpropionamide] (Standard)
|
Reference Standards
|
|
|
Antioxidant 1098 (Standard) is the analytical standard of Antioxidant 1098. This product is intended for research and analytical applications.
|
-
- HY-100832A
-
|
|
Histone Methyltransferase
|
Cancer
|
|
UNC3866 TFA is a potent antagonist of the CBX7-H3 interaction as determined by AlphaScreen (IC50=66±1.2 nM) and is more than 100-fold selective for CBX7 over the other nine members of this methyl-lysine (Kme) reader panel.
|
-
- HY-172625
-
|
|
E3 Ligase Ligand-Linker Conjugates
|
Cancer
|
|
VH 101-amide-piperidine-Pip-alkyne is an E3 Ligase Ligand-Linker Conjugates that can be used to synthesize PROTAC degrader. The linker part of VH 101-amide-piperidine-Pip-alkyne is tert-Butyl 4-ethynyl-[1,4'-bipiperidine]-1'-carboxylate (HY-W442074), and the VHL-type E3 ubiquitinase ligand is VH 101, acid (HY-47070) .
|
-
- HY-75473
-
|
|
Drug Intermediate
|
Others
|
|
(R)-tert-Butyl 4-(4-(6-amino-5-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)pyridin-3-yl)-1H-pyrazol-1-yl)piperidine-1-carboxylate is a drug intermediate for synthesis of various active compounds.
|
-
- HY-170828
-
|
|
PROTACs
SWI/SNF Complex
|
Others
|
|
SMD-1087 is a PROTAC that selectively targets SMARCA2 (DC50=8 nM, Dmax=89%) and SMARCA4 with a DC50 of 1 μM. SMD-1087 consists of the E3 ligase ligand (S,R,S)-AHPC-Me (blue part) (HY-112078), the target protein ligand SMI-1074 (red part) (HY-170817), and the PROTAC linker (1r,4r)-tert-Butyl 4-(bromomethyl)cyclohexanecarboxylate (black part) (HY-W890392). Among them, its target protein ligand + Linker part corresponds to SMARCA2 Ligand-Linker Conjugate-1 (HY-170829) .
|
-
- HY-114402
-
|
|
PROTACs
Androgen Receptor
|
Cancer
|
ARD-69 is a PROTAC degrader based on the E3 ubiquitin ligase VHL and targeting the androgen receptor, which can induce androgen receptor (AR) protein degradation in AR-positive prostate cancer cells. ARD-69 inhibits AR-regulated gene expression, binds to the AR ligand binding domain at one end and binds to VHL at the other end, prompting AR to be recruited to the E3 ubiquitin ligase complex, triggering proteasome degradation, thereby inhibiting AR signaling pathways and downstream gene expression (such as PSA, TMPRSS2). ARD-69 can be used to study of castration-resistant prostate cancer (mCRPC) . ARD-69 is composed of a target protein ligand (pink part) AR antagonist 14 (HY-172624), a PROTAC linker (black part) tert-Butyl 4-ethynyl-[1,4'-bipiperidine]-1'-carboxylate (HY-W442074), and a VHL-type E3 ubiquitinase ligand (blue part) VH 101, acid (HY-47070); among them, the VHL ligand and the linker can form a conjugate VH 101-amide-piperidine-Pip-alkyne (HY-172625).
|
-
- HY-W108710R
-
|
tert-butyl [(4R,6S)-6-{(E)-2-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]ethenyl}-2,2-dimethyl-1,3-dioxan-4-yl]acetate (Standard)
|
Reference Standards
|
|
|
t-Butyl (3R,5S)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-isopropylidenedioxy-6-heptenoate (Standard) is the analytical standard of t-Butyl (3R,5S)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-3,5-isopropylidenedioxy-6-heptenoate. This product is intended for research and analytical applications.
|
-
| Cat. No. |
Product Name |
Type |
-
- HY-W007500
-
|
|
Biochemical Assay Reagents
|
|
2,6-Di-Tert-butyl-4-methylpyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
-
- HY-W003177
-
|
|
Biochemical Assay Reagents
|
|
tert-Butyl 4-iodopiperidine-1-carboxylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
|
| Cat. No. |
Product Name |
Target |
Research Area |
-
- HY-100832A
-
|
|
Histone Methyltransferase
|
Cancer
|
|
UNC3866 TFA is a potent antagonist of the CBX7-H3 interaction as determined by AlphaScreen (IC50=66±1.2 nM) and is more than 100-fold selective for CBX7 over the other nine members of this methyl-lysine (Kme) reader panel.
|
| Cat. No. |
Product Name |
Category |
Target |
Chemical Structure |
| Cat. No. |
Product Name |
Chemical Structure |
-
- HY-21376S
-
|
|
|
tert-Butyl 4-amino-1H-pyrazole-1-carboxylate-d2 is the deuterium labeled tert-Butyl 4-amino-1H-pyrazole-1-carboxylate.
|
-
-
- HY-76929S
-
|
|
|
tert-Butyl 4-aminobenzoate- 13C6 is the 13C labeled tert-Butyl 4-aminobenzoate .
|
-
-
- HY-W010037S
-
|
|
|
2-(tert-Butyl)-4-methoxyphenol-d3 is deuterium labeled 2-(tert-Butyl)-4-methoxyphenol.
|
-
-
- HY-W740068
-
|
|
|
tert-Butyl 4-Nitrophenyl Carbonate-d9 is the deuterium labeled Tert-Butyl (4-nitrophenyl) carbonate (HY-W683522).
|
-
-
- HY-W024365S
-
|
|
|
2-tert-Butyl-4-hydroxyanisole-d3 is deuterium labeled 3-tert-Butyl-4-methoxyphenol.
|
-
-
- HY-W700253
-
|
|
|
tert-Butyl 4-methylpiperazine-1-carboxylate-d8 is the deuterium labeled tert-Butyl 4-methylpiperazine-1-carboxylate (HY-W050208).
|
-
-
- HY-32208S
-
|
|
|
tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate-d4 is the deuterium labeled tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate[1].
|
-
-
- HY-W009359S
-
|
|
|
tert-Butyl 4-benzylpiperazine-1-carboxylate-d8 is the deuterium labeled tert-Butyl 4-benzylpiperazine-1-carboxylate .
|
-
-
- HY-W704049
-
|
|
|
tert-Butyl 4-(methyl-d3)piperazine-1-carboxylate is the deuterium labeled tert-Butyl 4-methylpiperazine-1-carboxylate (HY-W050208).
|
-
-
- HY-W283336S
-
|
|
|
2,5-Di-(tert-butyl)-4-methoxyphenol-3,6-d20 is the deuterium labeled 2,5-Di-tert-butyl-4-methoxyphenol .
|
-
-
- HY-W077436S
-
|
|
|
2,6-Di-(tert-butyl)-4-methoxyphenol-3,5-d20 is the deuterium labeled 2,6-Di-tert-butyl-4-methoxyphenol .
|
-
-
- HY-W077436S1
-
|
|
|
Butylated hydroxyanisole-d18 (2,6-Di-Tert-Butyl-4-Methoxyphenol-d18) is the deuterium labeled Butylated hydroxyanisole.
|
-
| Cat. No. |
Product Name |
|
Classification |
-
- HY-114402
-
|
|
|
PROTAC Synthesis
|
ARD-69 is a PROTAC degrader based on the E3 ubiquitin ligase VHL and targeting the androgen receptor, which can induce androgen receptor (AR) protein degradation in AR-positive prostate cancer cells. ARD-69 inhibits AR-regulated gene expression, binds to the AR ligand binding domain at one end and binds to VHL at the other end, prompting AR to be recruited to the E3 ubiquitin ligase complex, triggering proteasome degradation, thereby inhibiting AR signaling pathways and downstream gene expression (such as PSA, TMPRSS2). ARD-69 can be used to study of castration-resistant prostate cancer (mCRPC) . ARD-69 is composed of a target protein ligand (pink part) AR antagonist 14 (HY-172624), a PROTAC linker (black part) tert-Butyl 4-ethynyl-[1,4'-bipiperidine]-1'-carboxylate (HY-W442074), and a VHL-type E3 ubiquitinase ligand (blue part) VH 101, acid (HY-47070); among them, the VHL ligand and the linker can form a conjugate VH 101-amide-piperidine-Pip-alkyne (HY-172625).
|
Your information is safe with us. * Required Fields.
Inquiry Information
- Product Name:
- Cat. No.:
- Quantity:
- MCE Japan Authorized Agent: