6710-47-0

Basic information

• Product Name: 1-β-D-deoxyribofuranosyl-1,2-dihydropyrimidin-2-one
• CAS NO: 6710-47-0
• Molecular Weight: 212.205
• Mol File: 6710-47-0.mol

Chemical Properties

• CAS DataBase Reference: 1-β-D-deoxyribofuranosyl-1,2-dihydropyrimidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-β-D-deoxyribofuranosyl-1,2-dihydropyrimidin-2-one(6710-47-0)
• EPA Substance Registry System: 1-β-D-deoxyribofuranosyl-1,2-dihydropyrimidin-2-one(6710-47-0)

Safety Data

• Hazardous Substances Data: 6710-47-0(Hazardous Substances Data)

Upstream product

• 68753-36-6 1-<2'-Desoxy-3',5'-di-O-(p-toluoyl)-β-D-ribofuranosyl>-2(1H)-pyrimidinon 

Downstream Products

• 1092106-32-5 2'-deoxyzebularine 5'-[phenyl(benzoxy-L-alaninyl)]phosphate 
• 1092106-28-9 2'-deoxyzebularine 5'-[phenyl(methoxy-L-alaninyl)]phosphate 
• 1092106-30-3 2'-deoxyzebularine 5'-[4-chlorophenyl(ethoxy-L-alaninyl)]phosphate 
• 1092106-31-4 2'-deoxyzebularine 3',5'-bis[4-chlorophenyl(ethoxy-L-alaninyl)]phosphate 
• 1092106-40-5 2'-deoxyzebularine 5'-[naphthyl(benzoxydimethylglycininyl)]phosphate 
• 1092106-38-1 2'-deoxyzebularine 5'-[phenyl(benzoxydimethylglycininyl)]phosphate 
• 1092106-39-2 2'-deoxyzebularine 3',5'-bis[phenyl(benzoxydimethylglycininyl)]phosphate 
• 99152-54-2 2-Desoxy-β-D-ribofuranosyl-2(1H)-pyrimidinon-3'-<(2-chlorophenyl)-(2-cyanoaethyl)-phosphat> 
• 557-01-7 2-hydroxypyrimidine 
• 99152-51-9 1-(2'-Desoxy-5'-O-dimethoxytrityl-β-D-ribofuranosyl)-2(1H)-pyrimidinon 

Relevant articles and documents

Nucleoside und Nucleotide. Teil 15. Synthese von Desoxyribonucleosid-monophosphaten und -triphosphaten mit 2(1H)-Pyrimidinon, 2(1H)-Pyridinon und 4-Amino-2(1H)-pyridinon als Basen

The phosphorylation of the modified nucleosides 1-(2'-deoxy-β-D-ribofuranosyl)-2(1H)-pyrimidinone (Md, 4), 4-amino-1-(2'-deoxy-β-D-ribofuranosyl)-2(1H)-pyridinone (Zd, 6) and the synthesis of 1-(2'-deoxy-β-D-ribofuranosyl)-2(1H)-pyri

Efficient synthesis of 2′-deoxyzebularine and its α-anomer by the silyl method of N-glycosylation. Crystal structures and conformational study in solution

2′-Deoxyzebularine and its α-anomer have been efficiently synthesized with relatively high stereoselectivity by a modified procedure of the silyl method of the N-glycosidic bond formation. An SnCl4- catalyzed condensation of silylated pyrimidin

53. Nucleoside und Nucleotide. Teil 22. Synthese eines Tridecanucleosiddodecaphosphats, das die unnatuerliche Base 2(1H)-Pyrimidinon enthaelt

Nucleosides and Nucleotides.Part 22.Synthesis of a Tridecanucleoside Dodecaphosphate Containing the Unnatural Base 2(1H)-Pyrimidinone.The tridecanucleosid dodecaphosphate d(TpTpMpCpCpTpCpApApApApTpC) incorporating the modified nucleoside 1-(2'-deoxy-β-D-r