5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-methyl-, ethyl ester

Base Information

Chemical Name:5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-methyl-, ethyl ester
CAS No.:648889-07-0
Molecular Formula:C13H11Cl2NO2S
Molecular Weight:316.20300
Hs Code.:

Synonyms:5-Thiazolecarboxylic acid,2-(2,4-dichlorophenyl)-4-methyl-,ethyl ester;2-(2,4-dichloro-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester;

Suppliers and Price of 5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-methyl-, 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 5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-methyl-, ethyl ester

Chemical Property:

PSA：67.43000
LogP:4.60200

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-methyl-, ethyl ester

There total 2 articles about 5-Thiazolecarboxylic acid, 2-(2,4-dichlorophenyl)-4-methyl-, 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: 5.0%

: 2775-38-4
2,4-dichlorothiobenzamide

: 609-15-4
ethyl 2-chloro-3-oxo-butyrate

: 648889-07-0
2-(2,4-dichloro-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester

Guidance literature:: In ethanol; for 48h; Heating / reflux;

Reference yield:

: 2447-79-2
2,4-dichlorobenzamide

: 648889-07-0
2-(2,4-dichloro-phenyl)-4-methyl-thiazole-5-carboxylic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Lawessons reagent / toluene / 6 h / 60 °C / Inert atmosphere; Schlenk technique

2: ethanol / 4 h / Reflux

With Lawessons reagent; In ethanol; toluene;
DOI:10.1111/cbdd.12729