C₃₂H₃₆NO₁₂P

Base Information

Chemical Name:C₃₂H₃₆NO₁₂P
CAS No.:92054-26-7
Molecular Formula:C₃₂H₃₆NO₁₂P
Molecular Weight:657.611
Hs Code.:

C<sub>32</sub>H<sub>36</sub>NO<sub>12</sub>P

Synonyms:C₃₂H₃₆NO₁₂P

Suppliers and Price of C₃₂H₃₆NO₁₂P

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 C₃₂H₃₆NO₁₂P

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₂H₃₆NO₁₂P

There total 7 articles about C₃₂H₃₆NO₁₂P 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: 77.0%

: 87462-01-9
C₃₂H₃₄NO₁₁P

: 92054-26-7
C₃₂H₃₆NO₁₂P

Guidance literature:: In acetic acid; at 75 ℃; for 2h;
DOI:10.1021/ja00291a029

Reference yield:

: 87461-99-2
C₃₀H₂₉BrO₉

: 92054-26-7
C₃₂H₃₆NO₁₂P

Guidance literature:: Multi-step reaction with 6 steps

1: 96 percent / 1,5-diazabicyclo<4.3.0>non-5-ene (DBN) / benzene / 1 h / 25 °C

2: toluene / 10 h / 90 °C

3: trifluoroacetic acid / CH₂Cl₂; methanol / 1 h

4: 90 percent / triethylamine (Et₃N) / CH₂Cl₂ / 3.5 h / 0 °C

5: 2.) sodium hydride / 1.) benzene, 25 deg C, 20 h; 2.) THF, 25 deg C, 3 h

6: 77 percent / acetic acid / 2 h / 75 °C

With DBN; sodium hydride; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; acetic acid; toluene; benzene;
DOI:10.1021/ja00291a029

Reference yield:

: 87461-97-0
C₃₀H₂₈O₈

: 92054-26-7
C₃₂H₃₆NO₁₂P

Guidance literature:: Multi-step reaction with 7 steps

1: 92 percent / N-bromosuccinimide (NBS), H₂O, acetic acid / CH₂Cl₂ / 5 h / 25 °C

2: 96 percent / 1,5-diazabicyclo<4.3.0>non-5-ene (DBN) / benzene / 1 h / 25 °C

3: toluene / 10 h / 90 °C

4: trifluoroacetic acid / CH₂Cl₂; methanol / 1 h

5: 90 percent / triethylamine (Et₃N) / CH₂Cl₂ / 3.5 h / 0 °C

6: 2.) sodium hydride / 1.) benzene, 25 deg C, 20 h; 2.) THF, 25 deg C, 3 h

7: 77 percent / acetic acid / 2 h / 75 °C

With N-Bromosuccinimide; DBN; water; sodium hydride; acetic acid; triethylamine; trifluoroacetic acid; In methanol; dichloromethane; acetic acid; toluene; benzene;
DOI:10.1021/ja00291a029