5116-31-4

Basic information

• Product Name: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone
• Synonyms: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone
• CAS NO: 5116-31-4
• Molecular Weight: 539.541
• Mol File: 5116-31-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone(5116-31-4)
• EPA Substance Registry System: 1-(2,3,5-tri-O-benzoyl-β-D-ribofuranosyl)-2(1H)-pyridinone(5116-31-4)

Safety Data

• Hazardous Substances Data: 5116-31-4(Hazardous Substances Data)

Upstream product

• 142-08-5 2-hydroxypyridin 
• 1055317-41-3 2,3,5-tri-O-benzoyl-D-ribofuranosyl(N-phenyl)trifluoroacetimidate 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 142-08-5 2-Pyridone 
• 18292-04-1 2-(trimethylsilyloxy)pyridine 

Downstream Products

• 15354-20-8 1-(2',3'-di-O-benzoyl-β-D-ribofuranosyl)-2-oxo-1,2-dihydropyridine 
• 175911-24-7 1-[(2R,3R,4R,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-tetrahydro-furan-2-yl]-1H-pyridin-2-one 
• 175911-23-6 1-{(2R,3R,4S,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-3,4-dihydroxy-tetrahydro-furan-2-yl}-1H-pyridin-2-one 
• 5116-37-0 1-(β-D-ribofuranosyl)-2-pyridone 

Relevant articles and documents

An improved procedure for nucleoside synthesis using glycosyl trifluoroacetimidates as donors

Using glycosyl trifluoroacetimidates as donors and nitromethane (or acetonitrile) as solvent, silylation and subsequent glycosylation were realized in a 'one-pot' procedure to provide the corresponding nucleosides derivatives in high yields.{A figure is p

Synthesis of pyridinone ribonucleoside 3'-O-phosphoramidites and their incorporation into oligoribonucleotides

Protected pyridin-2- and pyridin-4-one ribonucleosides 3 and 9 were synthesized using a one-pot reaction of silylated bases with 1-O-acetyl-tri-O-benzoyl-β-D-ribofuranose (2) in the presence of CF3SO3SiMe3. The nucleosides were converted in 4 steps into 3'-O-phosphoramidites 7 and 11 which were incorporated into hammerhead ribozyme substrates using solid-phase phosphoramidite chemistry.