7724-09-6

Basic information

• Product Name: 2-Hydroxybenzyl beta-D-glucopyranoside
• Synonyms: 2-Hydroxybenzyl beta-D-glucopyranoside
• CAS NO: 7724-09-6
• Molecular Formula: C₁₃H₁₈O₇
• Molecular Weight: 286.28
• Mol File: 7724-09-6.mol
• Article Data: 5

Chemical Properties

• Melting Point: 67-69 °C
• Boiling Point: 532.8±50.0 °C(Predicted)
• Appearance: /
• Density: 1.51
• PKA: 9.67±0.30(Predicted)
• CAS DataBase Reference: 2-Hydroxybenzyl beta-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Hydroxybenzyl beta-D-glucopyranoside(7724-09-6)
• EPA Substance Registry System: 2-Hydroxybenzyl beta-D-glucopyranoside(7724-09-6)

Safety Data

• Hazardous Substances Data: 7724-09-6(Hazardous Substances Data)

Usage

Description

2-Hydroxybenzyl beta-D-glucopyranoside is a natural phenolic compound consisting of a glucose molecule attached to a hydroxybenzyl group. It is found in various plant sources and has been the subject of research for its potential health benefits.

Uses

Used in Pharmaceutical Industry:
2-Hydroxybenzyl beta-D-glucopyranoside is used as a therapeutic agent for its antioxidant and anti-inflammatory properties, making it a potential candidate for treating conditions related to oxidative stress and inflammation.
Used in Diabetes Management:
2-Hydroxybenzyl beta-D-glucopyranoside is used as a compound for regulating blood sugar levels and improving insulin sensitivity, showing promise in the management of diabetes and metabolic syndrome.

Upstream product

• 15921-67-2 (2-hydroxy-benzyl)-(tetra-O-acetyl-β-D-glucopyranoside) 
• 89-95-2 2-methyl-benzyl alcohol 
• 57-50-1 Sucrose 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 2280-44-6 D-Glucose 
• 90-01-7 salicylic alcohol 
• 2492-87-7 4-nitrophenyl-β-D-glucoside 
• 1464-44-4 phenyl-β-D-glucopyranoside 

Downstream Products

• 492-62-6 alpha-D-glucopyranose 
• 90-01-7 salicylic alcohol 

Relevant articles and documents

Enzymatic resolution of (RS)-1-phenylalkyl β-D-glucosides to (R)-1-phenylalkyl β-primeverosides and (S)-1-phenylalkyl β-D-glucosides via plant xylosyltransferase

The stereoselective xylosylation of (RS)-1-phenylalkyl β-D-glucosides was investigated using plant xylosyltransferase isolated from cultured Catharanthus roseus cells. Enzymatic xylosylation of (RS)-1-phenylethyl β-D-glucoside afforded (R)-1-phenylethyl β

Simple synthesis of β-D-glycopyranosides using β-glycosidase from almonds

Enzymatic glycosidation of twenty-one kinds of alcohols (n-hepanol, n-octanol, 2-phenylethanol, 3-phenylpropanol, 4-phenylbutanol, 5-phenylpentanol, 6-phenylhexanol, furfury alcohol, 2-pyridinemethanol, isobutanol, isopentanol, p-methoxycinnamylalcohol) including secondary alcohols (isopropanol, cyclohexanol, 1-phenylethanol) and 1, ω-alkanediols (1,5-pentanediol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol), salicyl alcohol and 4-nitrophenyl β-D-glucopyranoside (5) using β-glucosidase from almonds stereoselectively gave the corresponding β-D-glucopyranosides in moderate yield.

Synthesis of β-Alkyl Glucosides by Enzymic Transglucosylation

Lactase from Kluyveromyces lactis was found to have high transglucosylation activity, transferring the glucosyl group of aryl glucoside to an alcoholic hydroxyl group in high yield.Both primary and secondary alcohols can accept the glucosyl group.Transglucosylation to glycol yielded a single kind of glucoside.A very hydrophilic alcohol, such as glycerol, could not serve as a substrate in this system.Hydrophobic alcohols slightly soluble in water were glucosylated in a two-phase system consisting of water and an organic solvent immiscible with water.Keywords - transglucosylation; transglycosylation; β-glucoside; lactase; Kluyveromyce s lactis; phenyl β-D-glucopyranoside; hydrophobic alcohol; two-phase system; alkyl glucoside; enzymic transglucosylation