303127-80-2

Basic information

• Product Name: 4-METHOXYPHENYL 3-O-BENZYL-BETA-D-GLUCOPYRANOSIDE
• Synonyms: 4-METHOXYPHENYL 3-O-BENZYL-BETA-D-GLUCOPYRANOSIDE;4-Methoxyphenyl 3-O-Benzyl-β-D-glucopyranoside;4-Methoxyphenyl 3-O-Benzyl-β(2R,3R,4S,5R,6S)-4-(Benzyloxy)-2-(hydroxymethyl)-6-(4-methoxyphenoxy)tetrahydro-2H-pyran-3,5-diol
• CAS NO: 303127-80-2
• Molecular Formula: C₂₀H₂₄O₇
• Molecular Weight: 376.4
• Product Categories: Biochemistry;Glucose;Glycosides;Sugars
• Mol File: 303127-80-2.mol
• Article Data: 2

Chemical Properties

• Melting Point: 141.0 to 146.0 °C
• Boiling Point: 599.163°C at 760 mmHg
• Flash Point: 316.163°C
• Appearance: /
• Density: 1.337g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.613
• Storage Temp.: Freezer
• PKA: 12.61±0.70(Predicted)
• CAS DataBase Reference: 4-METHOXYPHENYL 3-O-BENZYL-BETA-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXYPHENYL 3-O-BENZYL-BETA-D-GLUCOPYRANOSIDE(303127-80-2)
• EPA Substance Registry System: 4-METHOXYPHENYL 3-O-BENZYL-BETA-D-GLUCOPYRANOSIDE(303127-80-2)

Safety Data

• Hazardous Substances Data: 303127-80-2(Hazardous Substances Data)

Usage

General Description

4-Methoxyphenyl 3-O-benzyl-beta-D-glucopyranoside is a chemical compound with the molecular formula C21H24O8. It is a glycoside, which is a sugar molecule attached to a non-sugar moiety. 4-METHOXYPHENYL 3-O-BENZYL-BETA-D-GLUCOPYRANOSIDE is used in organic and medicinal chemistry for its potential biological activities, such as antioxidant, anti-inflammatory, and antimicrobial properties. It may also have applications in the development of pharmaceutical drugs and natural product synthesis. 4-Methoxyphenyl 3-O-benzyl-beta-D-glucopyranoside is a valuable molecule for further research and potential utilization in various scientific and industrial fields.

InChI:InChI=1/C20H24O7/c1-24-14-7-9-15(10-8-14)26-20-18(23)19(17(22)16(11-21)27-20)25-12-13-5-3-2-4-6-13/h2-10,16-23H,11-12H2,1H3/t16-,17-,18-,19+,20-/m1/s1

Upstream product

• 124-41-4 sodium methylate 
• 303127-79-9 4-Methoxyphenyl 2,4,6-tri-O-acetyl-3-O-benzyl-β-D-glucopyranoside 
• 39686-94-7 1,2,4,6-tetra-O-acetyl-3-O-benzyl-β-D-glucopyranose 
• 150-76-5 4-methoxy-phenol 

Downstream Products

• 303127-81-3 p-methoxyphenyl 3-O-benzyl-4,6-di-O-benzylidene-β-D-glucopyranoside 
• 303127-98-2 Benzyl O-(methyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosyluronate)-(1->3)-4-O-benzyl-6-O-(tert-butyldimethylsilyl)-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 303128-00-9 Benzyl O-(methyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosyluronate)-(1->3)-2-acetamido-4-O-benzyl-6-O-(tert-butyldimethylsilyl)-2-deoxy-β-D-galactopyranoside 
• 303127-99-3 Methyl O-(methyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosyluronate)-(1->3)-4-O-benzyl-6-O-(tert-butyldimethylsilyl)-2-deoxy-2-trichloroacetamido-β-D-galactopyranoside 
• 303128-01-0 Methyl O-(methyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosyluronate)-(1->3)-2-acetamido-4-O-benzyl-6-O-(tert-butyldimethylsilyl)-2-deoxy-β-D-galactopyranoside 
• 303128-02-1 Benzyl O-(methyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosyluronate)-(1->3)-2-acetamido-4-O-benzyl-2-deoxy-β-D-galactopyranoside 
• 303128-09-8 (2S,3S,4R,5R,6R)-6-((2R,3R,4R,5R,6R)-3-Acetylamino-2,5-bis-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-4-yloxy)-3,4-bis-benzyloxy-5-hydroxy-tetrahydro-pyran-2-carboxylic acid 
• 303128-03-2 Methyl O-(methyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosylunorate)-(1->3)-2-acetamido-4-O-benzyl-2-deoxy-β-D-galactopyranoside 
• 303128-10-1 (2S,3S,4R,5R,6R)-6-((2R,3R,4R,5R,6R)-3-Acetylamino-5-benzyloxy-6-hydroxymethyl-2-methoxy-tetrahydro-pyran-4-yloxy)-3,4-bis-benzyloxy-5-hydroxy-tetrahydro-pyran-2-carboxylic acid 
• 303127-85-7 Methyl 2-O-benzoyl-3,4-di-O-benzyl-1-O-trichloroacetimidoyl-α-D-glucopyrano 
• 303128-06-5 (2S,3S,4S,5R,6S)-5-Benzoyloxy-3,4-bis-benzyloxy-6-(4-methoxy-phenoxy)-tetrahydro-pyran-2-carboxylic acid 
• 303127-83-5 4-Methoxyphenyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranoside 
• 303127-84-6 Methyl (4-methoxyphenyl 2-O-benzoyl-3,4-di-O-benzyl-β-D-glucopyranosid)uronate 
• 303127-82-4 4-Methoxyphenyl 2-O-benzoyl-3-O-benzyl-4,6-O-benzylidene-β-D-glucopyranoside 

Relevant articles and documents

Toward the modular synthesis of glycosaminoglycans: Synthesis of hyaluronic acid disaccharide building blocks using a periodic acid oxidation

The synthesis of two differentially protected GluNAc-β(1→4)-GluA and GluA-β(1→3)-GluNAc disaccharide modules for the solid-phase assembly of hyaluronic acid are described. A periodic acid/chromium trioxide oxidation was the key transformation to facilitate access to the glucuronic acid moiety from glucose and should find wide application in the oxidation of primary alcohols.