359687-32-4

Basic information

• Product Name: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside
• Synonyms: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside
• CAS NO: 359687-32-4
• Molecular Weight: 655.761
• Mol File: 359687-32-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside(359687-32-4)
• EPA Substance Registry System: p-[2-[N-(p-vinylbenzyl)carbamoyl]ethyl]phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside(359687-32-4)

Safety Data

• Hazardous Substances Data: 359687-32-4(Hazardous Substances Data)

Upstream product

• 50325-49-0 p-vinylbenzylamine 
• 359687-15-3 p-(2-carboxyethyl)phenyl 4-O-acetyl-2-deoxy-2-fluoro-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 501-97-3 4-hydroxyphenylpropionic acid 
• 31770-76-0 3-(4-hydroxyphenyl)propionic acid benzyl ester 
• 3282-30-2 pivaloyl chloride 
• 359686-45-6 p-[2-(benzyloxycarbonyl)ethyl]phenyl β-D-galactopyranoside 
• 359686-52-5 p-[2-(benzyloxycarbonyl)ethyl]phenyl 3,6-di-O-pivaloyl-β-D-galactopyranoside 
• 359687-00-6 p-(2-carboxyethyl)phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359686-41-2 p-[2-(benzyloxycarbonyl)ethyl]phenyl 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoside 
• 359686-64-9 p-[2-(benzyloxycarbonyl)ethyl]phenyl 2,4-di-O-acetyl-3,6-di-O-pivaloyl-β-D-mannopyranoside 
• 359686-59-2 p-[2-(benzyloxycarbonyl)ethyl]phenyl 3,6-di-O-pivaloyl-2,4-bis(O-trifluoromethylsulfonyl)-β-D-galactopyranoside 

Relevant articles and documents

Synthesis of new glycopolymers containing β-d-mannopyranose, and c-2-substituted β-d-mannopyranose residues as a new class of inhibitor

New styryl monomers containing β-D-mannopyranose, 2-acetamido-2-deoxy-β-D-mannopyranose, 2-deoxy-2-fluoro-β-D-mannopyranose, and 2-deoxy-β-D-arabino-hexopyranose on their side chains, were efficiently synthesized as a new class of a potent inhibitor resistant to exo-α-mannosidase digestion. The binding affinity of the carbohydrate polymers obtained from those mannopyranosyl styryl monomers by radical polymerization with Concanavalin A were evaluated. A binding assay indicated that the multivalency effect and the affinity enhancement attained by modification at the C-2 position of the β-D-mannopyranoside residue resulted in the.