130288-81-2

Basic information

• Product Name: C₃₁H₃₂N₂O₉P^(1-)
• CAS NO: 130288-81-2
• Molecular Weight: 607.577
• Mol File: 130288-81-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: C₃₁H₃₂N₂O₉P^(1-)(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₁H₃₂N₂O₉P^(1-)(130288-81-2)
• EPA Substance Registry System: C₃₁H₃₂N₂O₉P^(1-)(130288-81-2)

Safety Data

• Hazardous Substances Data: 130288-81-2(Hazardous Substances Data)

Upstream product

• 13325-10-5 4-Aminobutanol 
• 102987-83-7 5′-O-(4,4′-dimethoxytrityl)thymidine-3′-O-[2-cyanoethyl]phosphonate 
• 4048-33-3 6-amino-1-hexanol 
• 141-43-5 ethanolamine 
• 129624-17-5 5'-O-dimethoxytritylthymidine 3'-hydrogenphosphonodithioate 
• 128981-11-3 C₃₅H₃₅N₈O₇P 
• 40615-39-2 5'-O-(4-4'-dimethoxytrityl)thymidine 
• 156-87-6 propan-1-ol-3-amine 
• 120104-57-6 bis(1,1,1,3,3,3-hexafluoropropan-2-yl) hydrogen phosphite 
• 66470-81-3 tris(1,1,1,3,3,3-hexafluoroisopropyl)phosphite 

Downstream Products

• 180475-92-7 2,4,6-Trichlorophenyl 5'-O-dimethoxytritylthymidin-3'-yl phosphonate 
• 114797-74-9 C₃₆H₃₆N₃O₉P 
• 908248-49-7 C₄₆H₅₃N₄O₁₀PSi 
• 307309-80-4 C₄₀H₄₂Cl₃N₂O₉PSi 
• 170638-52-5 5'-O-(dimethoxytrityl)thymidin-3'-yl (trimethylsilyl)-H-phosphonate 
• 182245-71-2 C₃₇H₄₉N₂O₉PSi₂ 
• 102987-86-0 C₄₈H₄₉N₄O₁₄P 
• 157793-51-6 3'-O-(4,4'-dimethoxytrityl)thymidin-5'-yl 5'-O-(4,4'-dimethoxytrityl)thymidin-3'-yl ethyl phosphonate 

Relevant articles and documents

A Convenient Approach to the Synthesis of Deoxyribonucleoside-3'-hydrogen Phosphonates via Bis(1,1,1,3,3,3-hexafluoro-2-propyl) Phosphonate Intermediate

Transesterification of a new reagent, bis(1,1,1,3,3,3-hexafluoro-2-propyl)phosphonates was found to be very effective for the preparation of deoxyribonucleoside-3'-hydrogen phosphonates.The yields of deoxyribooligonucleotides by the H-phosphonate method o

Oxidative and nonoxidative formation of internucleotide linkages

Activation of nucleoside 3'-hydrogenphosphonodithioates with iodine in the presence of nucleosides and amines yields dinucleoside phosphorodithioates and nucleoside phosphorodithioamidates, respectively. Similar activation of nucleoside 3'-methylphosphono

A CONVENIENT METHOD FOR THE SYNTHESIS OF DEOXYRIBONUCLEOSIDE 3'-HYDROGENPHOSPHONATES

Appropriately protected 5'-O-dimethoxytrityldeoxyribonucleoside derivatives were converted to the corresponding 3'-hydrogenphosphonates by treatment with phosphinic acid in the presence of mesitylenedisulfonyl chloride via an oxidative phosphonylation process.