102562-11-8

Basic information

• Product Name: 2',3',5'-tri-O-acetyl-8-bromo-O²,O⁶-bis<2-(p-nitrophenyl)ethyl>xanthosine
• Synonyms: 2',3',5'-tri-O-acetyl-8-bromo-O²,O⁶-bis<2-(p-nitrophenyl)ethyl>xanthosine
• CAS NO: 102562-11-8
• Molecular Weight: 787.535
• Mol File: 102562-11-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2',3',5'-tri-O-acetyl-8-bromo-O²,O⁶-bis<2-(p-nitrophenyl)ethyl>xanthosine(CAS DataBase Reference)
• NIST Chemistry Reference: 2',3',5'-tri-O-acetyl-8-bromo-O²,O⁶-bis<2-(p-nitrophenyl)ethyl>xanthosine(102562-11-8)
• EPA Substance Registry System: 2',3',5'-tri-O-acetyl-8-bromo-O²,O⁶-bis<2-(p-nitrophenyl)ethyl>xanthosine(102562-11-8)

Safety Data

• Hazardous Substances Data: 102562-11-8(Hazardous Substances Data)

Upstream product

• 15717-45-0 2',3',5'.-tri-O-acetyl-8-bromoguanosine 
• 4016-63-1 8-bromoguanosine 
• 102604-08-0 2',3',5'-tri-O-acetyl-8-bromo-O⁶-<2(-p-nitrophenyl)ethyl>guanosine 
• 100-27-6 2-(4-nitrophenyl)ethanol 
• 20264-96-4 2-(4-nitrophenyl)ethyl iodide 
• 102604-04-6 2',3',5'-tri-O-acetyl-8-bromo-O⁶-<2-(p-nitrophenyl)ethyl>xanthosine 

Downstream Products

• 102562-14-1 2,6,8-tris<2-(p-nitrophenyl)ethoxy>-9-(β-D-ribofuranosyl)-9H-purine 
• 102562-13-0 2',3',5'-tri-O-acetyl-2,6,8-tris<2-(p-nitrophenyl)ethoxy>-9-(β-D-ribofuranosyl)-9H-purine 
• 102562-15-2 5'-O-monomethoxytrityl-2,6,8-tris<2-(p-nitrophenyl)ethoxy>-9-(β-D-ribofuranosyl)-9H-purine 
• 21082-30-4 9-β-(D-ribofuranosyl)-1H-purine-2,6,8(3H,7H,9H)-trione 
• 102562-12-9 2',3',5'-tri-O-acetyl-2,6-bis<2-(p-nitrophenyl)ethoxy>-9-(β-D-ribofuranosyl)-7H-purin-8(9H)-one 

Relevant articles and documents

Nucleotides; Part XXXVI A New Synthesis of 9-(β-D-Ribofuranosyl)uric Acid and its 5'-Monophosphate

Syntheses for 9-(β-D-ribofuranosyl)uric acid (16) and its 5'-monophosphate 14 have been achieved starting from guanosine and applying the 2-(?-nitrophenyl)ethyl group for protection of the aglycon moiety as well as the phosphate function.A more effficient and direct approach to 14 uses O6,O8-dibenzyl protection and phosphorylation by the Yoshikawa procedure.The various protected intermediates have been characterized by spectroscopic means and elemental analysis.