35922-92-0

Basic information

• Product Name: N-(2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl)acetamide
• CAS NO: 35922-92-0
• Molecular Weight: 637.643
• Mol File: 35922-92-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N-(2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl)acetamide(35922-92-0)
• EPA Substance Registry System: N-(2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl)acetamide(35922-92-0)

Safety Data

• Hazardous Substances Data: 35922-92-0(Hazardous Substances Data)

Upstream product

• 33639-93-9 N-Methoxy-N-methyl (1,2,3,4-Di-O-isopropylidene-D-galactopyranose uronic acid) amide 
• 507-09-5 tiolacetic acid 
• 41093-30-5 2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl azide 
• 65864-61-1 β-D-mannopyranosyl azide 
• 65864-60-0 2,3,4,6-tetra-O-acetyl-1-azido-1-deoxy-β-D-mannopyranose 
• 33639-91-7 2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl amine 
• 1385026-77-6 N-(2,3,4,6-tetra-O-benzoyl-β-D-mannopyranosyl)-2,4-dinitrobenzenesulfonamide 
• 98-88-4 benzoyl chloride 
• 14218-11-2 2,3,4,6-tetra-O-benzoylglucosyl bromide 
• 2592-58-7 1,2,3,4,6-penta-O-benzoyl-D-glucopyranoside 
• 2280-44-6 D-Glucose 
• 108-24-7 acetic anhydride 
• 41093-31-6 (2R,3R,4S,5R,6R)-2-amino-6-((benzoyloxy)methyl)tetrahydro-2H-pyran-3,4,5-triyl tribenzoate 
• 13992-25-1 1-azido-1-deoxy-β-D-glucopyranoside tetraacetate 

Relevant articles and documents

Facile and efficient access to C1-aminosugar derivatives under mild conditions

A facile and efficient synthesis of C1-aminosugar derivatives under catalyst-free conditions is described here. In particular, readily available benzoyl glycosyl bromides react smoothly to give a broad scope of C1-aminosugar derivatives in good yields. Th

Method of producing an amide

The present invention discloses a new method for synthesizing an amide based on a fundamental mechanistic revision of the reaction of thio acids and organic azides. Moreover, the application of this method to the selective preparation of several classes of complex amides in nonpolar and polar solvents, including water, is provided.