3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile

Base Information

Chemical Name:3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile
CAS No.:641571-12-2
Molecular Formula:C12H8 F3 N3
Molecular Weight:251.211
Hs Code.:
Mol file:641571-12-2.mol

Synonyms:3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile

Suppliers and Price of 3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile

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

TRC
3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile
2.5mg
$ 250.00

Labseeker
-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile 95
5g
$ 1417.00

American Custom Chemicals Corporation
3-(4-METHYL-1H-IMIDAZOL-1-YL)-5-(TRIFLUOROMETHYL)BENZONITRILE 95.00%
5MG
$ 497.53

Alichem
3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile
1g
$ 998.00

Total 15 raw suppliers

Chemical Property of 3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile

Chemical Property:

PSA：41.61000
LogP:3.07118

Purity/Quality:

97% ^*data from raw suppliers

3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Uses 3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile acts as a reagent use in the synthesis of small molecular inhibitors that targets the catalytic domains of protein kinase that are not in active conformation.

Technology Process of 3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile

There total 3 articles about 3-(4-Methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile 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: 75.3%

: 822-36-6
4-methyl-1H-imidazole

: 149793-69-1
3-fluoro-5-trifluoromethyl-benzonitrile

: 641571-12-2
3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl)benzonitrile

Guidance literature:: 4-methyl-1H-imidazole; With sodium hydride; In 1-methyl-pyrrolidin-2-one; at 20 - 25 ℃; for 1h;

3-fluoro-5-trifluoromethyl-benzonitrile; In 1-methyl-pyrrolidin-2-one; at 20 - 25 ℃; for 2h;