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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!2025-02-06
331 Results for "
hydroxyl groups
" in MedChemExpress (MCE) Product Catalog:
Products (331)
331 Results for "hydroxyl groups" in MCE Product Catalog:
Cat. No.: HY-W460072
CAS No.: 86013-78-7
Target:
Research Areas:
tert-Butyl 7-hydroxyheptanoate is a linker with a hydroxyl group and a t-butyl ester. The hydroxyl group allows for further derivatization or replacement with many other reactive functional groups. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
Research Areas:
Hexamethoxymethylmelamine (Hexakis(methoxymethyl)melamine; HMMM) is a type of multifunctional melamine-formaldehyde crosslinker. Under acid-catalyzed conditions, Hexamethoxymethylmelamine enables chemical crosslinking between hydroxyl-functionalized polymers and hydroxyl groups in coating systems via methoxy-hydroxyl reactions, forming an interconnected network structure. Hexamethoxymethylmelamine can be used in organic synthesis-related research, such as thermosetting coatings .
Cat. No.: HY-W039729
CAS No.: 75178-90-4
Target:
Research Areas:
5-(Boc-amino)-1-pentanol is a linker containing a hydroxyl group and Boc-protected amino group. The hydroxyl group enables further derivatization or replacement with other reactive functional groups. The Boc group can be deprotected under mild acidic conditions to form the free amine.
Cat. No.: HY-174967C
Cat. No.: HY-W007345
CAS No.: 53981-24-1
Synonyms: 4-Fluoro-2-hydroxyaniline
Target:
Research Areas:
2-Amino-5-fluorophenol is an isomer of aminofluorophenol and also a HONO generator. 2-Amino-5-fluorophenol reacts with nitrogen dioxide (NO2) via two pathways to form nitrous acid (HONO): hydrogen abstraction from the hydroxyl group and hydrogen abstraction from the amino group, with both the amino and hydroxyl groups participating in the reaction in the transition state .
Cat. No.: HY-151822
CAS No.: 2566404-76-8
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Research Areas:
Hydroxy-PEG3-DBCO is a click chemistry reagent containing an azide group. Hydroxy-PEG3-DBCO is a PEG linker containing a DBCO moiety and a terminal primary hydroxyl group. The hydroxyl can react with a variety of functional groups and the hydrophilic PEG spacer arm can provide better solubility to labeled molecules. DBCO is commonly used for copper-free Click Chemistry reactions. Reagent grade, for research use only .
Cat. No.: HY-D1067
CAS No.: 1392488-07-1
Cat. No.: HY-W190921
CAS No.: 2100306-78-1
Target:
Research Areas:
t-Butyl 3-(hydroxypropoxyl)-propanoate contains reactive hydroxyl and t-butyl protected carboxyl moieties. The hydroxyl group can react to further derivatize the compound. The t-butyl carbonyl group can be deprotected under acidic conditions.
Cat. No.: HY-174963C
Cat. No.: HY-W800822
CAS No.: 6283-92-7
Synonyms: Lauryl lactate
Target:
Research Areas:
Lactic acid dodecyl ester (Lauryl lactate) is a lipid with a terminal hydroxyl group at the head. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
Cat. No.: HY-W174661
CAS No.: 73839-20-0
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Research Areas:
tert-Butyl 6-hydroxyhexanoate is a linker with a hydroxyl group and a t-butyl ester. The hydroxyl group allows for further derivatization or replacement with many other reactive functional groups. The t-butyl protected carboxyl group can be deprotected under acidic conditions.
Cat. No.: HY-W591962
CAS No.: 170220-11-8
Synonyms: 1-Pentanol, 5-azido-
Target:
Research Areas:
5-Azidopentan-1-ol (1-Pentanol, 5-azido-) is a linker containing an azide group and a terminal hydroxyl group. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
Cat. No.: HY-174967A
Cat. No.: HY-W250446
CAS No.: 56618-58-7
Target:
Research Areas:
(R)-Methyl 3-hydroxydecanoate is an enantiomerically pure hydroxylated fatty acid methyl ester. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
Cat. No.: HY-135580
CAS No.: 84541-38-8
Target:
Research Areas:
Raloxifene Bismethyl Ether is a metabolite of Raloxifene and an estrogen receptor inactive compound on which both hydroxyl groups are absent .
Cat. No.: HY-135580A
CAS No.: 84541-36-6
Target:
Research Areas:
Raloxifene Bismethyl Ether hydrochloride is a metabolite of Raloxifene and an estrogen receptor inactive compound on which both hydroxyl groups are absent .
Cat. No.: HY-W1120392
CAS No.: 29928-00-5
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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
