82469-69-0

Basic information

• Product Name: 3,4,6-tri-O-benzoyl-α-D-arabino-hexopyranosyl-2-ulose bromide
• Synonyms: 3,4,6-tri-O-benzoyl-α-D-arabino-hexopyranosyl-2-ulose bromide
• CAS NO: 82469-69-0
• Molecular Weight: 553.363
• Mol File: 82469-69-0.mol

Chemical Properties

• CAS DataBase Reference: 3,4,6-tri-O-benzoyl-α-D-arabino-hexopyranosyl-2-ulose bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,6-tri-O-benzoyl-α-D-arabino-hexopyranosyl-2-ulose bromide(82469-69-0)
• EPA Substance Registry System: 3,4,6-tri-O-benzoyl-α-D-arabino-hexopyranosyl-2-ulose bromide(82469-69-0)

Safety Data

• Hazardous Substances Data: 82469-69-0(Hazardous Substances Data)

Upstream product

• 82569-81-1 1,5-anhydro-3,4,6-tri-O-benzoyl-D-fructose oxime 
• 75414-32-3 1,5-anhydro-3,4,6-tri-O-benzoyl-D-fructose 
• 14125-75-8 2,3,4,6-tetra-O-benzoyl-D-hydroxyglucal 

Downstream Products

• 53495-62-8 C₂₂H₁₈O₈ 
• 53437-57-3 3,4,6-tri-O-benzoyl-α-D-glucopyranosyl bromide 
• 74629-56-4 1,5-anhydro-3,4,6-tri-O-benzoyl-D-glucitol 
• 562075-69-8 1,2:3,4-di-O-isopropylidene-6-O-(3',4',6'-tri-O-benzoyl-2-deoxy-β-D-arabino-hexopyranos-2-ulosyl)-D-galactopyranose 
• 835896-95-2 (2R,3R,4S,4aS,5aS,9aS,10aR)-3,4-bis(benzoyloxy)-2-(benzoyloxymethyl)-4a-hydroxy-decahydro-2H-pyrano[2,3-b][1,4]benzodioxin 
• 835896-96-3 (2R,3R,4S,4aR,5aS,9aS,10aR)-3,4-bis(benzoyloxy)-2-(benzoyloxymethyl)-4a-hydroxy-decahydro-2H-pyrano[2,3-b][1,4]benzodioxin 
• 1198604-71-5 1,2:3,4-di-O-isopropylidene-6-O-(3',4',6'-tri-O-benzoyl-2-deoxy-2-hydroxyimino-β-D-arabino-hexopyranosyl)-α-D-galactopyranose 
• 1198604-70-4 1,2:3,4-di-O-isopropylidene-6-O-(3',4',6'-tri-O-benzoyl-2-deoxy-2-hydroxyimino-β-D-arabino-hexopyranosyl)-α-D-galactopyranose 
• 1198604-72-6 1,2:3,4-di-O-isopropylidene-6-O-(3',4',6'-tri-O-benzoyl-2E-benzoyloxyimino-2-deoxy-β-D-arabino-hexopyranosyl)-α-D-galactopyranose 
• 127844-93-3 C₃₀H₂₄N₂O₈S 
• 87713-54-0 (2R,6S)-4-benzoyloxy-6-benzoyloxymethyl-2-cyclohexyloxy-2H-pyran-3(6H)-one 
• 87713-53-9 C₂₃H₂₂O₇ 
• 141514-08-1 3,4,6-tri-O-benzoyl-1-ethylsulfonyl-β-arabino-hexopyranosid-2-ulose 

Relevant articles and documents

Various glycosyl donors with a ketone or oxime function next to the anomeric centre: Facile preparation and evaluation of their selectivities in glycosidations

An efficient one-pot procedure is described for the conversion of a variety of hydroxyglycal esters to their 2-oxoglycosyl bromides which simply comprises of brief treatment with nN-bromosuccinimide/methanol at ambient temperature. Exhibiting comparably l

Sugar Enolones, XVIII. - Stereocontrolled Functionalization at Proanomeric Centres by Photobromination. - A Novel Efficient Access to Oxo- and Oximinoglycosyl Bromides

Suitably O-blocked monosaccharides carrying an electron acceptor group such as an oxo or oximino function next to a proanomeric centre, readily homolyze the corresponding push-pull-substituted C-H bond to give under photobromination conditions the respect