128262-40-8

Basic information

• Product Name: 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl chloride
• Synonyms: 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl chloride
• CAS NO: 128262-40-8
• Molecular Weight: 404.891
• Mol File: 128262-40-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl chloride(128262-40-8)
• EPA Substance Registry System: 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl chloride(128262-40-8)

Safety Data

• Hazardous Substances Data: 128262-40-8(Hazardous Substances Data)

Upstream product

• 134524-12-2 1,2-di-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranose 
• 14133-63-2 methyl 2,3-O-isopropylidene-α-D-rhamnopyranoside 
• 148431-61-2 methyl 2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 86447-92-9 methyl 4-O-benzyl-6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside 
• 100-44-7 benzyl chloride 
• 100-39-0 benzyl bromide 
• 125519-98-4 methyl 3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 109526-95-6 methyl 4-O-benzyl-6-deoxy-α-D-mannopyranoside 

Downstream Products

• 152174-29-3 ethyl 3,4-di-O-benzyl-2-O-(2',4'-di-O-benzyl-α-D-rhamnopyranosyl)-1-thio-α-D-rhamnopyranoside 
• 152174-34-0 ethyl 2-O-(3'-O-acetyl-2',4'-di-O-benzyl-α-D-rhamnopyranosyl)-3,4-di-O-benzyl-1-thio-α-D-rhamnopyranoside 
• 125519-98-4 methyl 3,4-di-O-benzyl-6-deoxy-α-D-mannopyranoside 
• 148431-62-3 1,2-anhydro-3,4-di-O-benzyl-6-deoxy-β-D-mannopyranose 
• 141936-83-6 Octyl 6-O-(2-O-acetyl-3,4-di-O-benzyl-6-deoxy-α-D-mannopyranosyl)-2,4-di-O-benzyl-β-D-mannopyranoside 
• 134407-33-3 ethyl 3,4-di-O-benzyl-1-thio-α-D-rhamnopyranoside 

Relevant articles and documents

Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-L- and β-D-rhamnopyranoses

1,2-Anhydro-3,4-di-O-benzyl-α-L-rhamnopyranose was synthesized from L-rhamnose, while the D-enantiomer was synthesized from methyl 6-deoxy-2,3-O-isopropylidene-α-D-mannopyranoside. For both of the syntheses, the key intermediates were 2-O-acetyl-3,4-di-O-