Final Thoughts on Chemistry for Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.SDS of cas: 72850-52-3, you can also check out more blogs about72850-52-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.72850-52-3, Name is Ethyl 2-chloro-4-(trifluoromethyl)thiazole-5-carboxylate, molecular formula is C7H5ClF3NO2S. In a Article，once mentioned of 72850-52-3, SDS of cas: 72850-52-3

A variety of 2-halo-5-thiazolecarboxylates was prepared from substituted-3-aminoacrylates and 3-ketoesters.Selective reduction of 2-chloro-5-thiazolecarboxylates 4a, 4i and 4j with sodium borohydride in ethanol provided the corresponding 2-halo-5-thiazolemethanols 27 – 29.Nucleophilic displacement on <2-chloro-4-(trifluoromethyl)-5-thiazolyl>methyl methanesulfonate (32c) occured selectivity at the 5-substituent to provide 2-chloro-4-(trifluoromethyl)-5-(heteroatom-substituted methyl)thiazoles 32d-f.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.SDS of cas: 72850-52-3, you can also check out more blogs about72850-52-3

Reference：
Thiazole | C3H8060NS – PubChem,
Thiazole | chemical compound | Britannica