84396-42-9

Basic information

• Product Name: 1-(5-O-triphenylmethyl-2,3-O-isopropylidene-α-D-ribofuranosyl)-5,6-dimethylbenzimidazole
• Synonyms: 1-(5-O-triphenylmethyl-2,3-O-isopropylidene-α-D-ribofuranosyl)-5,6-dimethylbenzimidazole
• CAS NO: 84396-42-9
• Molecular Weight: 560.693
• Mol File: 84396-42-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(5-O-triphenylmethyl-2,3-O-isopropylidene-α-D-ribofuranosyl)-5,6-dimethylbenzimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5-O-triphenylmethyl-2,3-O-isopropylidene-α-D-ribofuranosyl)-5,6-dimethylbenzimidazole(84396-42-9)
• EPA Substance Registry System: 1-(5-O-triphenylmethyl-2,3-O-isopropylidene-α-D-ribofuranosyl)-5,6-dimethylbenzimidazole(84396-42-9)

Safety Data

• Hazardous Substances Data: 84396-42-9(Hazardous Substances Data)

Upstream product

• 54503-64-9 2,3-O-isopropylidene-5-O-trityl-D-ribofuranose 
• 91275-64-8 5,6-dimethyl-1-(trimethylsilyl)-1H-benzimidazole 

Downstream Products

• 132-13-8 5,6-dimethyl-α-D-ribofuranosylbenzimidazole 
• 13082-84-3 5,6-Dimethyl-1-β-D-ribofuranosyl-benzimidazol 

Relevant articles and documents

Regioselective glycosylation: Synthesis of α-indoline nucleosides

Novel indoline ribonucleosides with the α-N-glycoside configuration are synthesized with very high regioselectivity in 90-96% yield, using TMS protected indolines and 2,3-O-(1-methylethylidene)-5-O-(triphenylmethyl)- α/β-D-ribofuranose. The structures of

Deprotection of α-imidazole/benzimidazole ribonucleosides by catalytic carbon tetrabromide initiated photolysis

Several protected benzimidazole and imidazole α-ribonucleosides were deprotected in excellent yield at ambient temperature using CBr4 initiated photolysis in methanol at ambient temperature. No selectivity was observed and both trityl and isopr