Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate

Base Information

Chemical Name:Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate
CAS No.:1260655-20-6
Molecular Formula:C14H12ClF3N2O2
Molecular Weight:332.71
Hs Code.:2933290090
Mol file:1260655-20-6.mol

Synonyms:Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate

Suppliers and Price of Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate

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

Crysdot
Ethyl1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate 95+%
1g
$ 416.00

Total 4 raw suppliers

Chemical Property of Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate

Chemical Property:

PSA：44.12000
LogP:3.78030

Purity/Quality:

98%Min ^*data from raw suppliers

Ethyl1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate

There total 2 articles about Ethyl 1-(4-chloro-3-(trifluoromethyl)benzyl)-1H-imidazole-4-carboxylate 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:

: 62039-92-3
4-chloro-3-(trifluoromethyl)benzylamine

: 87951-12-0
3-Dimethylamino-2-isocyanacrylsaeure-ethylester

: 1260655-20-6
C₁₄H₁₂ClF₃N₂O₂

Guidance literature:: In butan-1-ol; at 95 ℃;
DOI:10.1016/j.bmcl.2011.01.113

Reference yield:

: 2999-46-4
Ethyl isocyanoacetate

: 1260655-20-6
C₁₄H₁₂ClF₃N₂O₂

Guidance literature:: Multi-step reaction with 2 steps

1: N,N-dimethyl acetamide

2: butan-1-ol / 95 °C

In N,N-dimethyl acetamide; butan-1-ol;
DOI:10.1016/j.bmcl.2011.01.113