288585-01-3

Basic information

• Product Name: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside
• Synonyms: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside
• CAS NO: 288585-01-3
• Molecular Weight: 687.81
• Mol File: 288585-01-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside(288585-01-3)
• EPA Substance Registry System: phenyl 2-O-(allyl(dimethyl)silyl)-3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside(288585-01-3)

Safety Data

• Hazardous Substances Data: 288585-01-3(Hazardous Substances Data)

Upstream product

• 4028-23-3 Allylchlorodimethylsilane 
• 128775-56-4 phenyl 3,4,6-tri-O-benzyl-1-seleno-β-D-glucopyranoside 

Downstream Products

• 288584-96-3 3-C-(3,4,6-tri-O-benzyl-β-D-glucopyranosyl)1-propanol 

Relevant articles and documents

Stereoselective synthesis of α- and β-C-glucosides via radical cyclization with an allylsilyl tether. Control of the stereoselectivity by changing the conformation of the pyranose ring

An efficient method for preparing both 1α- and 1β-C-glucosides having a 3-hydroxypropyl group at the anomeric position via a radical cyclization reaction with an allylsilyl tether was developed. The stereoselectivity of the radical cyclization can be cont