CAS 19488-48-3
:methyl 2,3,6-tri-O-benzyl-alpha-D-glucopyranoside
Description:
Methyl 2,3,6-tri-O-benzyl-alpha-D-glucopyranoside is a glycoside derived from glucose, characterized by the presence of three benzyl groups attached to the hydroxyl positions at C-2, C-3, and C-6 of the glucopyranose ring, along with a methoxy group at the anomeric position. This compound is typically a white to off-white crystalline solid, exhibiting good solubility in organic solvents such as dichloromethane and methanol, but limited solubility in water due to its hydrophobic benzyl substituents. It is often used in organic synthesis and carbohydrate chemistry as a protective group for hydroxyl functionalities, facilitating further chemical transformations. The presence of the benzyl groups enhances the stability and lipophilicity of the molecule, making it useful in various applications, including drug development and the synthesis of complex carbohydrates. Additionally, its structure allows for potential interactions in biological systems, making it a subject of interest in medicinal chemistry.
Formula:C28H32O6
InChI:InChI=1/C28H32O6/c1-30-28-27(33-19-23-15-9-4-10-16-23)26(32-18-22-13-7-3-8-14-22)25(29)24(34-28)20-31-17-21-11-5-2-6-12-21/h2-16,24-29H,17-20H2,1H3/t24-,25-,26+,27-,28+/m1/s1
Synonyms:- a-D-Glucopyranoside, methyl 2,3,6-tri-O-(phenylmethyl)-
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Found 2 products.
Methyl 2,3,6-tri-O-benzyl-a-D-glucopyranoside
CAS:<p>Methyl 2,3,6-tri-O-benzyl-a-D-glucopyranoside is a reductive amine that can be used as an inhibitor of enzymes. The compound has been shown to inhibit the enzyme formate dehydrogenase. In addition, it has been found to inhibit other enzymes such as primary amines and reductive amination. Methyl 2,3,6-tri-O-benzyl-a-D-glucopyranoside is also a potential inhibitor of coupling reactions and anti HIV activity.</p>Formula:C28H32O6Purity:Min. 95%Molecular weight:464.22 g/mol
