135704-44-8

Basic information

• Product Name: C₃₆H₄₁N₂O₁₀P
• Synonyms: C₃₆H₄₁N₂O₁₀P
• CAS NO: 135704-44-8
• Molecular Weight: 692.703
• Mol File: 135704-44-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: C₃₆H₄₁N₂O₁₀P(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₆H₄₁N₂O₁₀P(135704-44-8)
• EPA Substance Registry System: C₃₆H₄₁N₂O₁₀P(135704-44-8)

Safety Data

• Hazardous Substances Data: 135704-44-8(Hazardous Substances Data)

Upstream product

• 3282-30-2 pivaloyl chloride 
• 3868-27-7 triethylammonium 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 50571-26-1 5'-O-dimethoxytritylthymidine 3'-H-phosphonate 
• 75-08-1 ethanethiol 

Downstream Products

• 173204-31-4 5'-O-dimethoxytritylthymidin-3'-yl trimethylsilyl H-phosphonothioate 
• 170638-52-5 5'-O-(dimethoxytrityl)thymidin-3'-yl (trimethylsilyl)-H-phosphonate 
• 135704-45-9 C₃₉H₄₉N₂O₁₀PSi 

Relevant articles and documents

Conversion of nucleoside H-phosphonate monoesters to the corresponding H- phosphonothioates. 31P NMR studies

31P NMR Studies on the conversion of nucleoside H-phosphonate monoesters into the corresponding H-phosphonothioates revealed that the key intermediate, the nucleoside trimethylsilyl pivaloyl phosphite 3, may undergo under the reaction condition

Aryl H-phosphonates. 6. Synthetic studies on the preparation of nucleoside N-alkyl-H-phosphonamidates

Various approaches to the synthesis of nucleoside H-phosphonamidates have been investigated. Direct couplings of nucleoside H-phosphonates with amines have been hampered by extensive reactions of the condensing agents with amines. Preactivation of nucleos