71397-61-0

Basic information

• Product Name: 4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide
• Synonyms: 4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide
• CAS NO: 71397-61-0
• Molecular Weight: 519.511
• Mol File: 71397-61-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide(71397-61-0)
• EPA Substance Registry System: 4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazide(71397-61-0)

Safety Data

• Hazardous Substances Data: 71397-61-0(Hazardous Substances Data)

Upstream product

• 29706-90-9 β-D-2,3,5-tri-O-benzoylribofuranosyl chloride 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 21823-89-2 2,3,5-tri-O-benzoyl-β-D-ribosyl isocyanate 

Downstream Products

• 80049-42-9 2,4-bis(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-1,2,4-triazolin-3-one 
• 80049-44-1 4-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-1,2,4-triazol-3(2H)-one 
• 82206-59-5 Methyl pyruvate (Z)-4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazone 
• 60432-13-5 Methyl glyoxylate (E)-4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazone 
• 82206-55-1 Methyl glyoxylate (Z)-4-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)semicarbazone 
• 98292-39-8 (E)-4-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-1-ethoxymethylenesemicarbazide 
• 98292-42-3 (Z)-4-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-1-(1-ethoxyethylidene)semicarbazide 
• 98292-43-4 (E)-4-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-1-(1-ethoxyethylidene)semicarbazide 
• 98292-40-1 4-(2,3,5-Tri-O-benzoyl-β-D-ribofuranosyl)-5-methyl-1,2,4-triazol-3(2H)-one 

Relevant articles and documents

Syntheses and Structure Assignments of Six Azolinone Ribonucleosides

N-Ribosidation of a series of azolinones was achieved via silylation and SnCl4 catalysis.N-Ribosidation of 4-imidazolin-2-one gave 1-β-D-ribofuranosyl-4-imidazolin-2-one; of 1,2,4-triazolin-3-one gave 2- and 4-β-D-ribofuranosyl-1,2,4-triazolin-3-one, and 2,4-di-β-D-ribofuranosyl-1,2,4-triazolin-3-one; and of 2-tetrazolin-5-one gave 1-β-D-ribofuranosyl-2-tetrazolin-5-one and 1,4-di-β-D-ribofuranosyl-2-tetrazolin-5-one.Structure assignments were based on NMR and mass spectra, microanalytical data, and interconversions.The triazolinone monoriboside isomer structures were differentiated by 13C NMR long-range coupling patterns, and the assignments were confirmed by X-ray crystallography.New syntheses were developed for several of the ribonucleosides by fashioning the azolinone rings from 2,3,5-tri-O-benzoylribofuranosyl isocyanate.