273935-08-3

Basic information

• Product Name: allyl 2,3,4-tri-O-benzyl-6-O-[4-(tert-butoxycarbonyl)benzyl]-α-D-glucopyranoside
• Synonyms: allyl 2,3,4-tri-O-benzyl-6-O-[4-(tert-butoxycarbonyl)benzyl]-α-D-glucopyranoside
• CAS NO: 273935-08-3
• Molecular Weight: 680.838
• Mol File: 273935-08-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: allyl 2,3,4-tri-O-benzyl-6-O-[4-(tert-butoxycarbonyl)benzyl]-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: allyl 2,3,4-tri-O-benzyl-6-O-[4-(tert-butoxycarbonyl)benzyl]-α-D-glucopyranoside(273935-08-3)
• EPA Substance Registry System: allyl 2,3,4-tri-O-benzyl-6-O-[4-(tert-butoxycarbonyl)benzyl]-α-D-glucopyranoside(273935-08-3)

Safety Data

• Hazardous Substances Data: 273935-08-3(Hazardous Substances Data)

Upstream product

• 78184-40-4 1-O-allyl-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 108052-76-2 4-(bromomethyl)benzoic acid 1,1-dimethylethyl ester 

Downstream Products

• 273935-10-7 2,3,4-tri-O-benzyl-6-O-[4-(tert-butoxycarbonyl)benzyl]-α-D-glucopyranosyl trichloroacetimidate 

Relevant articles and documents

Highly efficient synthesis of 1-thioglycosides in solution and solid phase using iminophosphorane bases

Disaccharides of 1-thioglycosides, an important class of glycomimics, can be synthesized by direct S-alkylation in exceptionally high yields when iminophosphorane bases are employed. The reaction conditions employed appear to be general and stereospecific