160056-33-7

Basic information

• Product Name: Thymidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 3'-(phenyl phosphonate)
• CAS NO: 160056-33-7
• Molecular Formula: C37H37N2O9P
• Molecular Weight: 684.683
• Mol File: 160056-33-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Thymidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 3'-(phenyl phosphonate)(CAS DataBase Reference)
• NIST Chemistry Reference: Thymidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 3'-(phenyl phosphonate)(160056-33-7)
• EPA Substance Registry System: Thymidine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-, 3'-(phenyl phosphonate)(160056-33-7)

Safety Data

• Hazardous Substances Data: 160056-33-7(Hazardous Substances Data)

Upstream product

• 50571-26-1 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 108-95-2 phenol 
• 3868-27-7 triethylammonium 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 4712-55-4 diphenyl hydrogen phosphite 
• 40615-39-2 5'-O-(4-4'-dimethoxytrityl)thymidine 

Downstream Products

• 1053647-07-6 C₅₁H₅₅N₈O₁₄P 
• 1053706-19-6 C₄₈H₅₇N₈O₁₄P 
• 1055039-22-9 C₄₇H₅₅N₈O₁₄P 
• 1053633-87-6 C₄₅H₅₁N₈O₁₄P 
• 637014-44-9 C₄₁H₄₄N₇O₁₂P 
• 50571-26-1 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 3868-27-7 triethylammonium 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 57538-74-6 phenyl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl phosphate 

Relevant articles and documents

Synthesis and resolution of dinucleotide(TpAZT) phosphoramidates

Dinucleotide (TpAZT) phosphoramidates were synthesized through Atherton-Todd reaction of dinucleoside H-phosphonates and amino acid methyl esters, and their diastereomers (Rp and Spu) were separated by crystallization. It was showed that the cheap methyl esters of natural alanine and phenylalanine could act as new chiral auxiliaries for large-scale synthesis of dinucleotide analogs.

31p NMR studies on oxidative transformations of aryl nucleoside h-phosphonate diesters

Various aspects of oxidative coupling of nucleoside aryl H-phosphonate diesters with nucleosides to produce important synthetic intermediates in the phosphotriester approach to oligonucleotide synthesis, dinucleoside aryl phosphotriesters, was investigated. Copyright

Aryl H-phosphonates. 8. Simple and efficient method for the preparation of nucleoside B-phosphonothioate monoesters

An efficient method for the preparation of nucleoside 3'-H- phosphonothioate monoesters was developed. It consists of phosphonylation of suitably protected nucleosides with diphenyl H-phosphonate to produce nucleoside phenyl H-phosphonates, followed by th