763123-25-7

Basic information

• Product Name: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{(2R,4aR,6S,7R,8R,8aS)-7-azido-6-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxycarbonylamino}-tetrahydro-pyran-3-yl ester
• CAS NO: 763123-25-7
• Molecular Weight: 808.912
• Mol File: 763123-25-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{(2R,4aR,6S,7R,8R,8aS)-7-azido-6-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxycarbonylamino}-tetrahydro-pyran-3-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{(2R,4aR,6S,7R,8R,8aS)-7-azido-6-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxycarbonylamino}-tetrahydro-pyran-3-yl ester(763123-25-7)
• EPA Substance Registry System: Acetic acid (2R,3R,4S,5R,6R)-4,5-diacetoxy-6-acetoxymethyl-2-{(2R,4aR,6S,7R,8R,8aS)-7-azido-6-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yloxycarbonylamino}-tetrahydro-pyran-3-yl ester(763123-25-7)

Safety Data

• Hazardous Substances Data: 763123-25-7(Hazardous Substances Data)

Upstream product

• 104974-80-3 Acetic acid (2R,3R,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-isocyanato-tetrahydro-pyran-4-yl ester 
• 157488-91-0 thexyldimethylsilyl 2-azido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 66118-22-7 (2R,3R,4S,5R,6R)-2-(acetoxymethyl)-6-isocyanotetrahydro-2H-pyran-3,4,5-triyl triacetate 

Relevant articles and documents

Synthesis of novel pseudodisaccharides and neoglycoconjugates containing an N-glycosyl carbamate backbone

A new class of pseudodisaccharides is presented in which a N-glycosyl carbamate is connected to a monosaccharide unit, using a mild and stereo-controlled isocyanide approach. The methodology was extended to the case of neoglycoconjugates useful as synthons for the construction of molecules with potential therapeutic interest.