Brief introduction of 161797-99-5

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.Quality Control of: Ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate, you can also check out more blogs about161797-99-5

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.161797-99-5, Name is Ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate, molecular formula is C13H13NO3S. In a Patent，once mentioned of 161797-99-5, Quality Control of: Ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate

Substituted thiazoles

This invention is directed to processes for making substituted thiazoles. The substituted thiazole, ethyl 2-(4-hydroxyphenyl)-4-methyl-1,3-thiazole-5-carboxylate, also known as TEI-6720, is useful for treatment of gout and hyperuricemia. This compound belongs to a class of substituted thiazoles that inhibit xanthine oxidase and thus block uric acid production.

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.Quality Control of: Ethyl 2-(4-hydroxyphenyl)-4-methylthiazole-5-carboxylate, you can also check out more blogs about161797-99-5

Reference：
Thiazole | C3H7787NS – PubChem,
Thiazole | chemical compound | Britannica