90762-86-0

Basic information

• Product Name: benzyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-glucopyranoside
• Synonyms: benzyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-glucopyranoside
• CAS NO: 90762-86-0
• Molecular Weight: 322.358
• Mol File: 90762-86-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-glucopyranoside(90762-86-0)
• EPA Substance Registry System: benzyl 3,4-di-O-acetyl-2,6-dideoxy-α-D-glucopyranoside(90762-86-0)

Safety Data

• Hazardous Substances Data: 90762-86-0(Hazardous Substances Data)

Upstream product

• 89063-61-6 1,3,4-Tri-O-acetyl-2,6-didesoxy-D-arabino-hexopyranose 
• 100-51-6 benzyl alcohol 
• 92611-14-8 benzyl 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-mannopyranoside 
• 92611-21-7 benzyl 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-glucopyranoside 
• 78138-31-5 3,4-di-O-acetyl-2,6-dibromo-2,6-dideoxy-α-D-glucopyranosyl bromide 
• 474017-59-9 benzyl 3,4-di-O-acetyl-2-bromo-2,6-dideoxy-α-D-mannopyranoside 
• 76739-66-7 3,4-di-O-acetyl-D-rhamnal 
• 78185-01-0 2,6-dideoxy-α-D-arabino-hexopyranose 

Downstream Products

• 474017-77-1 (+)-benzyl 3-(O-t-butyldimethylsilyl)-4-(O-mesyl)-2,6-dideoxy-α-D-glucopyranoside 
• 474017-73-7 benzyl 3-O-(tert-butyldimethylsilyl)-2,6-dideoxy-α-D-glucopyranoside 
• 474017-81-7 benzyl 4-O-mesyl-2,6-dideoxy-α-D-glucopyranoside 
• 474018-04-7 benzyl 3,4-anhydro-2,6-dideoxy-α-D-allopyranoside 
• 474017-85-1 benzyl 3,4-anhydro-2,6-dideoxy-α-D-galactopyranoside 
• 75810-07-0 Benzyl 2,6-Dideoxy-α-D-arabino-hexopyranoside 

Relevant articles and documents

Regiochemical control of the ring opening of 1,2-epoxides by means of chelating processes. Part 17: Synthesis and opening reactions of cis- and trans-oxides derived from (2S,6R)-2-benzyloxy-6-methyl-3,6-dihydro-2H-pyran, (2R,6R)- and (2S,6R)-2-methoxy-6-m

The regiochemical behavior of the title deoxy anhydrosugars, prepared in an enantioselective way starting from methyl α-D-glucopyranoside, was examined in opening reactions, both under standard and chelating conditions. The results clearly indicate the in

Preparation of α- and β-Linked Disaccharides of 2,6-Dideoxy-D-arabino-hexose. Synthesis of Bamflalactone

1,4-α-Linked disaccharides of 2,6-dideoxy-D-arabino-hexose are prepared from the selectively protected 2,6-dideoxy sugars 3 or 4 and the 1,5-anhydrohex-1-enitol (9) by using the N-iodosuccinimide (NIS) method or from the deoxy sugar 6 and the acetylated 2