A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 53137-27-2, Name is 2,4-Dimethylthiazole-5-carboxylic acid, molecular formula is C6H7NO2S. In a Article，once mentioned of 53137-27-2, Safety of 2,4-Dimethylthiazole-5-carboxylic acid
An iron-catalyzed oxidative esterification reaction between unactivated C(sp3)-H bonds from symmetric and asymmetric ethers and carboxylic acids using di-tert-butyl peroxide (DTBP) as the oxidant via a cross dehydrogenative coupling (CDC) reaction was established, which tolerates a wide range of cyclic ether substrates to react with aromatic acids and phenylacetic acid, providing an efficient method for the preparation of alpha-acyloxy ethers with good to excellent yields. Intermolecular competing kinetic isotope effect (KIE) experiments were also carried out, which indicate that C(sp 3)-H bond cleavage may be the rate-determining step of this CDC reaction.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 2,4-Dimethylthiazole-5-carboxylic acid. In my other articles, you can also check out more blogs about 53137-27-2
Reference：
Thiazole | C3H1681NS – PubChem,
Thiazole | chemical compound | Britannica