ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-carboxylate

Base Information

Chemical Name:ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-carboxylate
CAS No.:851224-80-1
Molecular Formula:C12H9F3N2O2S
Molecular Weight:302.277
Hs Code.:
Mol file:851224-80-1.mol

Synonyms:ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-carboxylate

Suppliers and Price of ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-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

Total 1 raw suppliers

Chemical Property of ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-carboxylate

Chemical Property:

PSA：80.32000
LogP:3.40060

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-carboxylate

There total 2 articles about ethyl 3-(4-(trifluoromethyl)phenyl)-1,2,4-thiadiazole-5-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: 92.0%

: 851224-79-8
5-(4-trifluoromethylphenyl)[1,3,4]oxathiazol-2-one

: 623-49-4
ethyl cyanoformate

: 851224-80-1
3-(4-trifluoromethylphenyl)[1,2,4]thiadiazole-5-carboxylic acid ethyl ester

Guidance literature:: In 1,2-dichloro-benzene; at 160 ℃; for 20h;
DOI:10.1021/jm070511x

Reference yield:

: 1891-90-3
p-trifluoromethylbenzamide

: 851224-80-1
3-(4-trifluoromethylphenyl)[1,2,4]thiadiazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 39 percent / toluene / 15 h / 60 °C

2: 92 percent / 1,2-dichloro-benzene / 20 h / 160 °C

In 1,2-dichloro-benzene; toluene;
DOI:10.1021/jm070511x