861695-56-9

Basic information

• Product Name: benzyl O-(2-O-benzoyl-4-O-benzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside
• Synonyms: benzyl O-(2-O-benzoyl-4-O-benzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside
• CAS NO: 861695-56-9
• Molecular Weight: 936.025
• Mol File: 861695-56-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzyl O-(2-O-benzoyl-4-O-benzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl O-(2-O-benzoyl-4-O-benzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside(861695-56-9)
• EPA Substance Registry System: benzyl O-(2-O-benzoyl-4-O-benzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside(861695-56-9)

Safety Data

• Hazardous Substances Data: 861695-56-9(Hazardous Substances Data)

Upstream product

• 861695-55-8 benzyl O-(2-O-benzoyl-4,6-O-benzylidene-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside 
• 861695-53-6 benzyl O-(2-O-acetyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside 
• 861695-54-7 benzyl O-(2-O-benzoyl-4,6-O-benzylidene-3-O-p-methoxybenzyl-β-D-mannopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalamido-β-D-glucopyranoside 
• 80035-36-5 benzyl 3,6-di-O-benzyl-2-deoxy-2-phthalimido-beta-D-glucopyranoside 

Downstream Products

• 1449039-89-7 benzyl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-α-D-mannopyranosyl-(1→3)-[2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-α-D-mannopyranosyl-(1→6)]-2-O-benzoyl-4-O-benzyl-β-D-mannopyranosyl-(1→4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 

Relevant articles and documents

Chemoenzymatic synthesis and lectin recognition of a selectively fluorinated glycoprotein Dedicated to Professor Benjamin G. Davis on the occasion of his receiving the Tetrahedron Young Investigator Award

A chemoenzymatic glycosylation remodeling method for the synthesis of selectively fluorinated glycoproteins is described. The method consists of chemical synthesis of a fluoroglycan oxazoline and its use as donor substrate for endoglycosidase (ENGase)-cat

Highly efficient endoglycosidase-catalyzed synthesis of glycopeptides using oligosaccharide oxazolines as donor substrates

A highly efficient chemoenzymatic synthesis of N-glycopeptides was achieved. It was found that using synthetic oligosaccharide oxazolines, the mimics of the presumed oxazolinium ion intermediate formed in a retaining mechanism of substrate-assisted cataly