2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Base Information

Chemical Name:2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate
CAS No.:305368-32-5
Molecular Formula:C₄₆H₇₉N₂O₁₀P
Molecular Weight:851.114
Hs Code.:

Synonyms:2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Suppliers and Price of 2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

There total 3 articles about 2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 57.0%

: 58670-89-6
2-decylteradecanol

: C₂₂H₃₀ClN₂O₉P

: 305368-32-5
2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 4h;
DOI:10.1016/S0960-894X(00)00396-6

Reference yield:

: 268227-43-6
ethyl (4-nitrophenyl)[11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl]phosphonate

: 305368-32-5
2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Guidance literature:: Multi-step reaction with 3 steps

1: CH₂Cl₂ / 48 h / 20 °C

2: (COCl)2 / CH₂Cl₂ / 2 h / 0 - 20 °C

3: 57 percent / Et₃N / CH₂Cl₂ / 4 h / 20 °C

With oxalyl dichloride; triethylamine; In dichloromethane; 1: Silylation / 2: Chlorination / 3: Esterification;
DOI:10.1016/S0960-894X(00)00396-6

Reference yield:

: C₂₅H₃₉N₂O₁₀PSi

: 305368-32-5
2-decyltetradecvyl (4-nitrophenyl) [11-([(2,5-dioxotetrahydro-1H-1-pyrrolyl)oxy]carbonyloxy)undecyl] phosphonate

Guidance literature:: Multi-step reaction with 2 steps

1: (COCl)2 / CH₂Cl₂ / 2 h / 0 - 20 °C

2: 57 percent / Et₃N / CH₂Cl₂ / 4 h / 20 °C

With oxalyl dichloride; triethylamine; In dichloromethane; 1: Chlorination / 2: Esterification;
DOI:10.1016/S0960-894X(00)00396-6