95087-12-0

Basic information

• Product Name: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,5-dihydro-4H-pyrazolo<3,4-d>pyrimidine-4-one
• Synonyms: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,5-dihydro-4H-pyrazolo<3,4-d>pyrimidine-4-one
• CAS NO: 95087-12-0
• Molecular Weight: 252.23
• Mol File: 95087-12-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,5-dihydro-4H-pyrazolo<3,4-d>pyrimidine-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,5-dihydro-4H-pyrazolo<3,4-d>pyrimidine-4-one(95087-12-0)
• EPA Substance Registry System: 1-(2-deoxy-β-D-erythro-pentofuranosyl)-1,5-dihydro-4H-pyrazolo<3,4-d>pyrimidine-4-one(95087-12-0)

Safety Data

• Hazardous Substances Data: 95087-12-0(Hazardous Substances Data)

Upstream product

• 5399-92-8 4-chloro-1H-pyrazolo[3,4-d]pyrimidine 

Relevant articles and documents

Synthesis and Hydrolytic Stability of 4-Substituted Pyrazolopyrimidine 2'-Deoxyribofuranosides

Phase-transfer glycosylation of 4-chloro-1H-pyrazolopyrimidine (1) with 2-deoxy-3,5-di-O-(p-toluoyl)-α-D-erythro-pentofuranosyl chloride (2) yielded the N-1 glycosylation product (3) in 42 percent.The protected intermediate (3) was converted into pyrazolopyrimidine 2'-deoxyribofuranosides with amino, oxo, and thioxo substituents at C-4.Kinetic data of proton-catalysed hydrolysis showed that pyrazolopyrimidine 2'-deoxyribofuranosides are more stable at the N-glycosylic bond than are the parent purine nucleosides.