127844-91-1

Basic information

• Product Name: C-(3,4,6-tri-O-benzoyl-β-D-arabino-hexopyranos-2-ulosyl)methanol
• Synonyms: C-(3,4,6-tri-O-benzoyl-β-D-arabino-hexopyranos-2-ulosyl)methanol
• CAS NO: 127844-91-1
• Molecular Weight: 534.519
• Mol File: 127844-91-1.mol

Chemical Properties

• CAS DataBase Reference: C-(3,4,6-tri-O-benzoyl-β-D-arabino-hexopyranos-2-ulosyl)methanol(CAS DataBase Reference)
• NIST Chemistry Reference: C-(3,4,6-tri-O-benzoyl-β-D-arabino-hexopyranos-2-ulosyl)methanol(127844-91-1)
• EPA Substance Registry System: C-(3,4,6-tri-O-benzoyl-β-D-arabino-hexopyranos-2-ulosyl)methanol(127844-91-1)

Safety Data

• Hazardous Substances Data: 127844-91-1(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 82469-69-0 3,4,6-tri-O-benzoyl-α-D-arabino-hexopyranosyl-2-ulose bromide 

Relevant articles and documents

C-glycosidations of a 2-ketohexosyl bromide with electrophilic, radical, and nucleophilic anomeric carbons

The susceptibility of acylated 2-ketohexosyl halides to Chomologation is demonstrated with the easily accessible tri-O-benzoyl-α-D-arabino-hexos-ulosyl bromide 1 as the model compound. C-Glycosidation with an electrophilic anomeric carbon requires prior c

Acylated 2-oxoglycosyl bromides: Exploration of their reaction potential

Acylated glycos-2-ulosyl bromides give a variety of useful ensuing reactions, preparatively most relevant being their smooth α- and β-selective glycosidation, their reduction to glucosyl bromides with a free 2-OH, and their C-homologation to higher-carbon