32742-28-2

Basic information

• Product Name: 2-methylphenyl-tetra-O-acetyl-α-D-glucopyranoside
• Synonyms: 2-methylphenyl-tetra-O-acetyl-α-D-glucopyranoside
• CAS NO: 32742-28-2
• Molecular Weight: 438.431
• Mol File: 32742-28-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-methylphenyl-tetra-O-acetyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-methylphenyl-tetra-O-acetyl-α-D-glucopyranoside(32742-28-2)
• EPA Substance Registry System: 2-methylphenyl-tetra-O-acetyl-α-D-glucopyranoside(32742-28-2)

Safety Data

• Hazardous Substances Data: 32742-28-2(Hazardous Substances Data)

Upstream product

• 122186-40-7 2-(2,3,4,6-tetra-O-acetyl-β-_D-glucopyranozyloxy)benzyl alcohol 
• 95-48-7 ortho-cresol 
• 604-69-3 β-D-glucose pentaacetate 
• 60523-66-2 2-(2,3,4,6-tetra-О-acetyl-β-d-glucopyranosyloxy)benzyl bromide 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Downstream Products

• 161767-48-2 2-methyl-6-nitrophenyl tetra-O-acetyl-α-D-glucopyranoside 
• 161767-52-8 2-methyl-4-nitrophenyl tetra-O-acetyl-β-D-glucopyranoside 
• 115431-91-9 (2R,3R,4S,5R,6S)-3,4,5-Trimethoxy-2-methoxymethyl-6-(2-methyl-cyclohexa-1,4-dienyloxy)-tetrahydro-pyran 
• 115431-89-5 (2R,3R,4S,5R,6S)-3,4,5-Trimethoxy-2-methoxymethyl-6-o-tolyloxy-tetrahydro-pyran 
• 138-52-3 D-(-)-salicin 
• 60523-66-2 2-(2,3,4,6-tetra-О-acetyl-β-d-glucopyranosyloxy)benzyl bromide 
• 7234-31-3 o-tolyl-β-D-glucopyranoside 
• 53829-49-5 (2-aminomethyl-phenyl)-β-D-glucopyranoside 
• 122186-40-7 2-(2,3,4,6-tetra-O-acetyl-β-_D-glucopyranozyloxy)benzyl alcohol 
• 161767-40-4 2-(fluoromethyl)phenyl α-D-glucopyranoside 
• 143836-12-8 2-bromomethyl-4-nitrophenyl tetra-O-acetyl-α-D-glucopyranoside 
• 143836-13-9 2-chloromethyl-4-nitrophenyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 
• 143836-10-6 2-chloromethyl-4-nitrophenyl α-D-glucopyranoside 
• 161767-45-9 2-(chloromethyl)phenyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside 

Relevant articles and documents

Selective demethylation ofO-aryl glycosides by iridium-catalyzed hydrosilylation

The cleavage of alkyl ethers by hydrosilylation is a powerful synthetic tool for the generation of silyl ethers. Previous attempts to apply this transformation to carbohydrate derivatives have been constrained by poor selectivity and preferential reductio

STEREOSELECTIVITY OF REACTIONS AT THE GLYCOSYDIC CENTER OF CARBOHYDRATES. V. SYNTHESIS OF 1,2-TRANS-ARYLGLYCOSIDES BY THE HELFERICH METHOD USING CATALYSIS BY ORTHOPHOSPHORIC ACID

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