1199797-32-4

Basic information

• Product Name: O⁴,O⁶-(R)-benzylidene-O¹,O³-dimethyl-β-D-arabino-[2]hexosul-1,5-ose
• CAS NO: 1199797-32-4
• Molecular Weight: 294.304
• Mol File: 1199797-32-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: O⁴,O⁶-(R)-benzylidene-O¹,O³-dimethyl-β-D-arabino-[2]hexosul-1,5-ose(CAS DataBase Reference)
• NIST Chemistry Reference: O⁴,O⁶-(R)-benzylidene-O¹,O³-dimethyl-β-D-arabino-[2]hexosul-1,5-ose(1199797-32-4)
• EPA Substance Registry System: O⁴,O⁶-(R)-benzylidene-O¹,O³-dimethyl-β-D-arabino-[2]hexosul-1,5-ose(1199797-32-4)

Safety Data

• Hazardous Substances Data: 1199797-32-4(Hazardous Substances Data)

Upstream product

• 110715-30-5 methyl 4,6-O-benzylidene-2-O-methyl-β-D-glucopyranoside 
• 70144-57-9 methyl 4,6-O-benzylidene-3-O-methyl-β-D-glucopyranoside 

Downstream Products

• 1152487-04-1 methyl 4,6-O-benzylidene-3-O-methyl-β-D-mannopyranoside 
• 30695-04-6 O³-methyl-D-arabino-[2]hexosulose-bis-phenylhydrazone 

Relevant articles and documents

Highly functionalized, enantiomerically pure furo[x,y-c]pyrans via alkylidenecarbenes derived from sugar templates: synthesis and mechanism study via computational chemistry

The new method for the generation of alkylidenecarbenes based on the reaction of trimethylsilylazide/Bu2SnO with α-cyanomesylates has been applied to readily available sugar derivatives for the synthesis of highly functionalized, enantiomerical

Synthesis of monodeoxy and mono-O-methyl congeners of methyl β-d-mannopyranosyl-(1→2)-β-d-mannopyranoside for epitope mapping of anti-Candida albicans antibodies

A panel of six complementary monodeoxy and mono-O-methyl congeners of methyl β-d-mannopyranosyl-(1→2)-β-d-mannopyranoside (1) were synthesized by stereoselective glycosylation of monodeoxy and mono-O-methyl monosaccharide acceptors with a 2-O-acetyl-gluco