257936-60-0

Basic information

• Product Name: methyl O-(2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
• Synonyms: methyl O-(2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside
• CAS NO: 257936-60-0
• Molecular Weight: 1327.92
• Mol File: 257936-60-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: methyl O-(2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl O-(2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside(257936-60-0)
• EPA Substance Registry System: methyl O-(2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-β-D-galactopyranosyl)-(1->4)-O-(2,3,6-tri-O-benzyl-β-D-glucopyranosyl)-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside(257936-60-0)

Safety Data

• Hazardous Substances Data: 257936-60-0(Hazardous Substances Data)

Upstream product

• 155786-86-0 methyl 2,3,6-tri-O-benzyl-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-benzyl-β-D-glucopyranoside 
• 257936-58-6 phenyl 2,3-di-O-benzoyl-4-O-chloroacetyl-6-deoxy-1-thio-β-D-galactopyranoside 
• 257936-53-1 phenyl 2,3-di-O-benzoyl-6-deoxy-1-thio-β-D-galactopyranoside 
• 257936-51-9 phenyl 2-O-benzoyl-6-deoxy-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside 
• 101696-00-8 phenyl 6-deoxy-3,4-O-isopropylidene-1-thio-β-D-galactopyranoside 
• 141193-62-6 Phenyl-2,3,4-tri-O-acetyl-6-desoxy-1-thio-β-D-galactopyranosid 
• 1214-98-8 phenyl 1-thio-β-D-fucopyranoside 

Relevant articles and documents

β-Acarbose. VIII the synthesis of some N-linked carba-oligosacchandes

Two carbohydrate triflates have been used to alkylate a 1-epivalienamine derivative to give small amounts of the desired secondary amines, in addition to amounts of the products of elimination. Deprotection of the secondary amines afforded a carba-disacch