86883-43-4

Basic information

• Product Name: 3-β-cholestanyl 2,3,5-tri-O-benzyl-α-D-ribofuranoside
• Synonyms: 3-β-cholestanyl 2,3,5-tri-O-benzyl-α-D-ribofuranoside
• CAS NO: 86883-43-4
• Molecular Weight: 791.168
• Mol File: 86883-43-4.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 3-β-cholestanyl 2,3,5-tri-O-benzyl-α-D-ribofuranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 3-β-cholestanyl 2,3,5-tri-O-benzyl-α-D-ribofuranoside(86883-43-4)
• EPA Substance Registry System: 3-β-cholestanyl 2,3,5-tri-O-benzyl-α-D-ribofuranoside(86883-43-4)

Safety Data

• Hazardous Substances Data: 86883-43-4(Hazardous Substances Data)

Upstream product

• 42995-55-1 3-β-cholestanyl trimethylsilyl ether 
• 91078-59-0 1-O-trimethylsilyl-2,3,5-tri-O-benzyl-D-arabinofuranose 
• 160549-10-0 2,3,5-tri-O-benzyl-D-arabinofuranose 
• 80-97-7 Cholestanol 
• 86883-51-4 2,3,5-tri-O-benzyl-α-L-arabinofuranosyl fluoride 
• 86883-41-2 2,3,5-tri-O-benzyl-α-D-ribofuranosyl fluoride 
• 16838-89-4 2,3,5-tri-O-benzyl-D-ribofuranose 
• 18880-51-8 (5α-cholestan-3β-yloxy)trimethylsilane 
• 91110-24-6 Acetic acid (2S,3R,4R,5R)-3,4-bis-benzyloxy-5-benzyloxymethyl-tetrahydro-furan-2-yl ester 
• 86883-42-3 2,3,5-tris-O-(phenylmethyl)-β-D-ribofuranosyl fluoride 
• 17608-41-2 cholestanol 

Relevant articles and documents

An efficient glycosylation reaction of 1-hydroxy sugars with various nucleophiles using a catalytic amount of activator and hexamethyldisiloxane

In the presence of hexamethyldisiloxane and anhydrous calcium sulfate, a catalytic amount of activator such as tin(II) trifluoromethanesulfonate, ytterbium trifluoromethanesulfonate, lanthanum trifluoromethanesulfonate or tin(II) chloride smoothly promote

Stereoselective Synthesis of 1,2-cis-Arabinofuranosides Using a New Titanium Catalyst

In the presence of catalytic amounts of oxotitanium and trimethylsilyl triflate, 1-O-trimethylsilyl-2,3,5-tri-O-benzyl-D-arabinofuranose stereoselectively reacts with various trimethylsilyl ethers to afford the corresponding 1

Stereoselective 1,2-cis Glycosylation Reaction of 1-O-Acetylribose with Silylated Nucleophiles by the Promotion of a New Catalyst System

1,2-cis-Ribofuranosides are stereoselectively prepared in high yields by the reaction of 1-O-acetyl-β-D-ribose with silylated nucleophiles by the promotion of a new catalyst system, the combined use of a catalytic amount of tin(IV) chloride and tin(II) tr