1104513-35-0

Basic information

• Product Name: p-methoxyphenyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside
• Synonyms: p-methoxyphenyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside
• CAS NO: 1104513-35-0
• Molecular Weight: 508.568
• Mol File: 1104513-35-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: p-methoxyphenyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-methoxyphenyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside(1104513-35-0)
• EPA Substance Registry System: p-methoxyphenyl 4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside(1104513-35-0)

Safety Data

• Hazardous Substances Data: 1104513-35-0(Hazardous Substances Data)

Upstream product

• 631-57-2 Acetyl cyanide 
• 159922-50-6 4-methoxyphenyl 2,6-di-O-benzyl-β-D-galactopyranoside 
• 159922-67-5 4-methoxyphenyl 3,4-O-isopropylidene-β-D-galactopyranoside 
• 1445-45-0 Trimethyl orthoacetate 
• 159922-68-6 4-methoxyphenyl 2,6-di-O-benzyl-3,4-O-isopropylidene-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 

Downstream Products

• 1616968-80-9 p-methoxyphenyl 2,3-di-O-benzoyl-6-O-benzyl-β-D-glucopyranosyl-(1 → 3)-4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside 
• 1262589-19-4 p-methoxyphenyl 2,3-di-O-benzoyl-4,6-O-benzylidene-β-D-glucopyranosyl-(1→3)-4-O-acetyl-2,6-di-O-benzyl-β-D-galactopyranoside 

Relevant articles and documents

Regioselective acylation of diols and triols: The cyanide effect

Central topics of carbohydrate chemistry embrace structural modifications of carbohydrates and oligosaccharide synthesis. Both require regioselectively protected building blocks that are mainly available via indirect multistep procedures. Hence, direct pr

Efficient acylation and sulfation of carbohydrates using sulfamic acid, a mild, eco-friendly catalyst under organic solvent-free conditions

A fast and efficient acylation of carbohydrate derivatives and free sugars using a stoichiometric quantity of acylating agents in the presence of sulfamic acid, an environmentally benign catalyst, under organic solvent-free conditions is reported. Excellent yields in the selective acylation and sulfation of carbohydrate derivatives have also been achieved using sulfamic acid as the catalyst. The reaction is fast and the yields were excellent.