C₄₀H₃₀NO₁₂P

Base Information

Chemical Name:C₄₀H₃₀NO₁₂P
CAS No.:572913-36-1
Molecular Formula:C₄₀H₃₀NO₁₂P
Molecular Weight:747.651
Hs Code.:

C<sub>40</sub>H<sub>30</sub>NO<sub>12</sub>P

Synonyms:C₄₀H₃₀NO₁₂P

Suppliers and Price of C₄₀H₃₀NO₁₂P

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 C₄₀H₃₀NO₁₂P

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₀H₃₀NO₁₂P

There total 7 articles about C₄₀H₃₀NO₁₂P 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: 96.0%

: 6066-82-6
1-hydroxy-pyrrolidine-2,5-dione

: 572913-34-9
C₃₆H₂₇O₁₀P

: 572913-36-1
C₄₀H₃₀NO₁₂P

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In chloroform; at 20 ℃; for 2h;
DOI:10.1002/chem.200390167

Reference yield:

: 108549-23-1
Dibenzyl N,N-diisopropylphosphoramidite

: 572913-36-1
C₄₀H₃₀NO₁₂P

Guidance literature:: Multi-step reaction with 3 steps

1: Et₃N; 1H-tetrazole / CHCl₃ / 0.5 h / 20 °C

2: 400 mg / mCPBA / CHCl₃ / 0.5 h / 20 °C

3: 96 percent / EDC*HCl / CHCl₃ / 2 h / 20 °C

With 1H-tetrazole; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; In chloroform;
DOI:10.1002/chem.200390167

Reference yield:

: 76608-15-6
6-carboxyfluorescein

: 572913-36-1
C₄₀H₃₀NO₁₂P

Guidance literature:: Multi-step reaction with 6 steps

1: 52 percent / H₂SO₄ / Heating

2: Cs₂CO₃ / dimethylformamide / 0.33 h / 20 °C

3: 110 mg / aq. NaOH / methanol / 1 h / 20 °C

4: Et₃N; 1H-tetrazole / CHCl₃ / 0.5 h / 20 °C

5: 400 mg / mCPBA / CHCl₃ / 0.5 h / 20 °C

6: 96 percent / EDC*HCl / CHCl₃ / 2 h / 20 °C

With 1H-tetrazole; sodium hydroxide; sulfuric acid; caesium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; 3-chloro-benzenecarboperoxoic acid; In methanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1002/chem.200390167