2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

Base Information

Chemical Name:2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester
CAS No.:405195-41-7
Molecular Formula:C₁₉H₁₇I₂NO₂
Molecular Weight:545.158
Hs Code.:

Synonyms:2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

Suppliers and Price of 2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

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-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

There total 3 articles about 2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester 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: 32.0%

: 2999-46-4
Ethyl isocyanoacetate

: 16004-15-2
1-bromomethyl-4-iodobenzene

: 405195-41-7
2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

Guidance literature:: With tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In acetonitrile; Heating;
DOI:10.1016/S0960-894X(01)00686-2

Reference yield:

: 624-31-7
4-tolyl iodide

: 405195-41-7
2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 87 percent / NBS; AIBN / CCl₄ / Heating; irradiation

2: 32 percent / K₂CO₃; tetrabutylammonium hydrogensulfate / acetonitrile

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; In tetrachloromethane; acetonitrile;
DOI:10.1107/S0108270103005183

Reference yield:

: 106-49-0,12221-03-3
p-toluidine

: 405195-41-7
2-(4-iodo-benzyl)-3-(4-iodo-phenyl)-2-isocyano-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: NaNO₂

1.2: 91 percent / KI

2.1: 87 percent / NBS; AIBN / CCl₄ / Heating; irradiation

3.1: 32 percent / K₂CO₃; tetrabutylammonium hydrogensulfate / acetonitrile

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); tetra(n-butyl)ammonium hydrogensulfate; potassium carbonate; sodium nitrite; In tetrachloromethane; acetonitrile;
DOI:10.1107/S0108270103005183