![tert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylate](https://file.medchemexpress.com/product_pic/hy-30536.gif "Click to View tert-Butyl 3,9-diazaspiro[5.5]undecane-3-carboxylate Product Detail")
![tert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate](https://file.medchemexpress.com/product_pic/hy-w043503.gif "Click to View tert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate Product Detail")
![3,9-Dimethyl-3,9-diazaspiro[5.5]undecane](https://file.medchemexpress.com/product_pic/hy-46871.gif "Click to View 3,9-Dimethyl-3,9-diazaspiro[5.5]undecane Product Detail")
![tert-Butyl 9-amino-3-azaspiro[5.5]undecane-3-carboxylate](https://file.medchemexpress.com/product_pic/hy-w056269.gif "Click to View tert-Butyl 9-amino-3-azaspiro[5.5]undecane-3-carboxylate Product Detail")
![3-Boc-3-azaspiro[5.5]undecane-9-carbaldehyde](https://file.medchemexpress.com/product_pic/hy-w056267.gif "Click to View 3-Boc-3-azaspiro[5.5]undecane-9-carbaldehyde Product Detail")
![3-(tert-Butoxycarbonyl)-3-azaspiro[5.5]undecane-9-carboxylic acid](https://file.medchemexpress.com/product_pic/hy-w059721.gif "Click to View 3-(tert-Butoxycarbonyl)-3-azaspiro[5.5]undecane-9-carboxylic acid Product Detail")
![3-Azaspiro[5.5]undecane-9-methanol](https://file.medchemexpress.com/product_pic/hy-159598.gif "Click to View 3-Azaspiro[5.5]undecane-9-methanol Product Detail")
![3-Azaspiro[5.5]undecane hydrochloride](https://file.medchemexpress.com/product_pic/hy-107755.gif "Click to View 3-Azaspiro[5.5]undecane hydrochloride Product Detail")
![1,7-Dioxaspiro[5.5]undecane](https://file.medchemexpress.com/product_pic/hy-w288838.gif "Click to View 1,7-Dioxaspiro[5.5]undecane Product Detail")
![3-Boc-3,9-Diazaspiro[5.5]undecane hydrochloride](https://file.medchemexpress.com/product_pic/hy-30533.gif "Click to View 3-Boc-3,9-Diazaspiro[5.5]undecane hydrochloride Product Detail")
![3-Benzyl-3,9-diazaspiro[5.5]undecane](https://file.medchemexpress.com/product_pic/hy-30534.gif "Click to View 3-Benzyl-3,9-diazaspiro[5.5]undecane Product Detail")
![3,9-Diazaspiro[5.5]undecane-3-carboxylic acid](https://file.medchemexpress.com/product_pic/hy-168912.gif "Click to View 3,9-Diazaspiro[5.5]undecane-3-carboxylic acid Product Detail")
![PIP-C-3-Azaspiro[5.5]undecane-boc](https://file.medchemexpress.com/product_pic/hy-161656.gif "Click to View PIP-C-3-Azaspiro[5.5]undecane-boc Product Detail")
![2-Methoxyphenyl dihydrouracil-azaspiro[5.5]undecane-C-PIP](https://file.medchemexpress.com/product_pic/hy-161657.gif "Click to View 2-Methoxyphenyl dihydrouracil-azaspiro[5.5]undecane-C-PIP Product Detail")
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23 Results for "
Undecane
" in MedChemExpress (MCE) Product Catalog:
Products (23)
23 Results for "Undecane" in MCE Product Catalog:
Cat. No.: HY-30536
CAS No.: 173405-78-2
Research Areas:
tert-Butyl 3,9-diazaspiroundecane-3-carboxylate is a 3,9-diazaspiroundecane-based building block and precursor for synthesizing γ-aminobutyric acid type A (GABAA) receptor antagonists .
Cat. No.: HY-W043503
CAS No.: 873924-08-4
Target:
Research Areas:
tert-Butyl 9-oxo-3-azaspiro[5.5]undecane-3-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
Cat. No.: HY-46871
CAS No.: 93004-48-9
Target:
Research Areas:
3,9-Dimethyl-3,9-diazaspiro[5.5]undecane is a rigid PROTAC linker can be used in the synthesis of PROTACs, such as FIP22 (HY-175764). FIP22 is a potent and selective IRAK4 PROTAC degrader with anti- atopic dermatitis activity .
Cat. No.: HY-W056269
CAS No.: 1272758-41-4
Target:
Research Areas:
tert-Butyl 9-amino-3-azaspiro[5.5]undecane-3-carboxylate is a PROTAC linker that can be used in the synthesis of PROTACs.
Cat. No.: HY-W056267
CAS No.: 1416176-14-1
Target:
Research Areas:
3-Boc-3-azaspiro[5.5]undecane-9-carbaldehyde is a PROTAC linker, and can be used for synthesis of PROTAC SOS1 degrader-8 (HY-161634) .
Cat. No.: HY-W005218
CAS No.: 765-04-8
Synonyms: 1,11-Undecanediol
Target:
Research Areas:
Undecane-1,11-diol (1,11-Undecanediol) is a PROTAC linker that can be used in the synthesis of PROTACs.
Cat. No.: HY-W059721
CAS No.: 170228-81-6
Target:
Research Areas:
3-(tert-Butoxycarbonyl)-3-azaspiro[5.5]undecane-9-carboxylic acid is a PROTAC linker that can be used in the synthesis of PROTACs.
Cat. No.: HY-159598
CAS No.: 1784372-01-5
Target:
Research Areas:
3-Azaspiro[5.5]undecane-9-methanol is a PROTAC linker. 3-Azaspiro[5.5]undecane-9-methanol can be used in synthesis CW-3308 (HY-159579) .
Synonyms: 4,4-Pentamethylenepiperidine hydrochloride
Target:
Research Areas:
3-Azaspiro[5.5]undecane (4,4-Pentamethylenepiperidine) hydrochloride is an inhibitor targeting the WT influenza A virus M2 (A/M2), with an IC50 of 1 μM .
Category:
Cat. No.: HY-122426S2
CAS No.: 1219802-82-0
Synonyms: Undecyl bromide-d4; Undecane, 1-bromo-d4
Cat. No.: HY-N8593S
CAS No.: 164858-54-2
Cat. No.: HY-W288838
CAS No.: 180-84-7
Category:
Target:
Cat. No.: HY-30533
CAS No.: 236406-47-6
Target:
Research Areas:
3-Boc-3,9-Diazaspiro[5.5]undecane (hydrochloride) is a PROTAC linker that can be used in the synthesis of PROTACs.
Cat. No.: HY-30534
CAS No.: 189333-49-1
Target:
Research Areas:
3-Benzyl-3,9-diazaspiro[5.5]undecane is a PROTAC linker that can be used in the synthesis of PROTACs.
Cat. No.: HY-168912
Target:
Research Areas:
3,9-Diazaspiro[5.5]undecane-3-carboxylic acid is the linker that can be used for synthesis of PROTAC c-Met degrader-3 (HY-168910) .
Cat. No.: HY-161656
CAS No.: 3027978-51-1
Target:
Research Areas:
PIP-C-3-Azaspiro[5.5]undecane-boc is the linker for PROTAC. PIP-C-3-Azaspiro[5.5]undecane-boc is utilized for synthesis of PROTAC SOS1 degrader-10 (HY-161654) .
Cat. No.: HY-161657
Research Areas:
2-Methoxyphenyl dihydrouracil-azaspiro[5.5]undecane-C-PIP is an E3 Ligase ligand-linker conjugate, and can be used for synthesis of PROTAC SOS1 degrader-10 (HY-161654) .
Cat. No.: HY-W131541
CAS No.: 937367-26-5
Target:
Research Areas:
tert-Butyl (11-aminoundecyl)carbamate is an alkane chain with terminal amine and Boc-protected amino groups. tert-Butyl (11-aminoundecyl)carbamate can be used as a PROTAC linker in the synthesis of PROTACs and other conjugation applications. Amine group is reactive with carboxylic acids, activated NHS esters, carbonyls (ketone, aldehyde) etc. The Boc group can be deprotected under mild acidic conditions to form the free amine.
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
