619328-21-1

Basic information

• Product Name: pent-4-enyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-β-D-glucopyranoside
• Synonyms: pent-4-enyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-β-D-glucopyranoside
• CAS NO: 619328-21-1
• Molecular Weight: 677.662
• Mol File: 619328-21-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: pent-4-enyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: pent-4-enyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-β-D-glucopyranoside(619328-21-1)
• EPA Substance Registry System: pent-4-enyl 2-azido-4,6-O-benzylidene-2-deoxy-3-O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-β-D-glucopyranoside(619328-21-1)

Safety Data

• Hazardous Substances Data: 619328-21-1(Hazardous Substances Data)

Upstream product

• 92420-89-8 methyl 2,3,4-tri-O-acetyl-1-O-(trichloroacetimidoyl)-α-D-glucopyranuronate 
• 72692-06-9 methyl 2,3,4-tri-O-acetyl-D-glucopyranuronate 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 171032-74-9 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-D-glucopyranose 
• 145840-43-3 3,4,6-tri-O-acetyl-2-azido-2-deoxy-D-glucopyranosyl trichloroacetimidate 

Downstream Products

• 619328-22-2 pent-4-enyl 4,6-O-benzylidene-2-deoxy-2-N-acetyl-3-O-(methyl 2,3,4-tri-O-acetyl-β-D-glucopyranosyluronate)-β-D-glucopyranoside 

Relevant articles and documents

Design and synthesis of hyaluronan-mimetic gemini disaccharides

An efficient strategy has been designed for the preparation of synthetic mimics of hyaluronan (HA, 1) and its dimerized (Gemini) disaccharides (2a,b) via n-pentenyl glycoside formation. Construction of the target molecules was achieved through a combination of protection/deprotection protocols, imidate glycosylation methodology followed by ozonolysis, and reductive amination. These tailored synthetic mimics could act as versatile building blocks with therapeutic applications in tissue engineering, treatment of cancer and as drug delivery agents.