508194-17-0

Basic information

• Product Name: allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-3-O-tert-butyldimethylsilyl-β-D-glucopyranoside
• Synonyms: allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-3-O-tert-butyldimethylsilyl-β-D-glucopyranoside
• CAS NO: 508194-17-0
• Molecular Weight: 463.646
• Mol File: 508194-17-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-3-O-tert-butyldimethylsilyl-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-3-O-tert-butyldimethylsilyl-β-D-glucopyranoside(508194-17-0)
• EPA Substance Registry System: allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-3-O-tert-butyldimethylsilyl-β-D-glucopyranoside(508194-17-0)

Safety Data

• Hazardous Substances Data: 508194-17-0(Hazardous Substances Data)

Upstream product

• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 63064-48-2 allyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 54400-75-8 allyl 2-acetamido-2-deoxy-β-D-glucopyranoside 
• 63064-49-3 allyl 2-acetamido-(R)-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 18162-48-6 tert-butyldimethylsilyl chloride 

Relevant articles and documents

Stereoselective synthesis of epoxyalkyl glycoside precursors of glycosyl glycerol analogues from alkenyl glycosides of N-acetyl-D-glucosamine derivatives

The synthesis of epoxyalkyl glycoside derivatives of N-acetyl-D-glucosamine is described. Epoxidation of the corresponding alkenyl glycosides with m-CPBA took place with different stereoselectivity depending on the nature of the unsaturated system and the protecting groups on the sugar moiety. The configuration of the newly formed stereogenic centres has been confirmed unequivocally by chemical correlation.