C₅₇H₁₀₁N₂O₆PSi

Base Information

• Chemical Name: C₅₇H₁₀₁N₂O₆PSi
• CAS No.: 115523-51-8
• Molecular Formula: C₅₇H₁₀₁N₂O₆PSi
• Molecular Weight: 969.498
• Mol file: 115523-51-8.mol

Synonyms:

Chemical Property of C₅₇H₁₀₁N₂O₆PSi

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of C₅₇H₁₀₁N₂O₆PSi

There total 8 articles about C₅₇H₁₀₁N₂O₆PSi 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:

Toluene-4-sulfonate(2-{[(E)-(2S,3S)-3-(tert-butyl-diphenyl-silanyloxy)-2-octadecanoylamino-octadec-4-enyloxy]-methoxy-phosphoryloxy}-ethyl)-trimethyl-ammonium; (115523-49-4,115589-59-8) → C57H101N2O6PSi (115523-51-8)

Guidance literature:

With trimethylamine; In toluene; for 12h; Ambient temperature;

Reference yield:

4-nitrophenyl stearate (14617-86-8) → C57H101N2O6PSi (115523-51-8)

Guidance literature:

Multi-step reaction with 5 steps

2: triethylamine / CHCl₃ / 0.5 h / Ambient temperature

3: tetrazole / acetonitrile; tetrahydrofuran / 3 h / Ambient temperature

4: t-butyl hydroperoxide / tetrahydrofuran; 2-methyl-propan-2-ol / 2 h

5: trimethylamine / toluene / 12 h / Ambient temperature

With 1H-tetrazole; tert.-butylhydroperoxide; triethylamine; trimethylamine; In tetrahydrofuran; chloroform; toluene; acetonitrile; tert-butyl alcohol;

Reference yield:

C23H47Al (41765-25-7) → C57H101N2O6PSi (115523-51-8)

Guidance literature:

Multi-step reaction with 6 steps

1: hexane; diethyl ether / 0.5 h / Ambient temperature; addition of reagent - 15 deg C

3: triethylamine / CHCl₃ / 0.5 h / Ambient temperature

4: tetrazole / acetonitrile; tetrahydrofuran / 3 h / Ambient temperature

5: t-butyl hydroperoxide / tetrahydrofuran; 2-methyl-propan-2-ol / 2 h

6: trimethylamine / toluene / 12 h / Ambient temperature

With 1H-tetrazole; tert.-butylhydroperoxide; triethylamine; trimethylamine; In tetrahydrofuran; diethyl ether; hexane; chloroform; toluene; acetonitrile; tert-butyl alcohol;

upstream raw materials:

Toluene-4-sulfonate(2-{[(E)-(2S,3S)-3-(tert-butyl-diphenyl-silanyloxy)-2-octadecanoylamino-octadec-4-enyloxy]-methoxy-phosphoryloxy}-ethyl)-trimethyl-ammonium;

4-nitrophenyl stearate

C₂₃H₄₇Al

threo-4-(1-hydroxy-2-hexadecenyl)-2-phenyl-Δ²-oxazoline