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. 76874-79-8, Name is 2-Amino-4-chlorothiazole-5-carbaldehyde, molecular formula is C4H3ClN2OS. In a Patent，once mentioned of 76874-79-8, name: 2-Amino-4-chlorothiazole-5-carbaldehyde
Compounds of the formula STR1 in which K is the radical of a coupling component of the aniline, alpha-naphthylamine, pyrazolone, aminopyrazole, indole, tetrahydroquinoline, thiazole, phenol, naphthol, pyridine or pyridone series. R is –CHO, –CH=C(CN)–R1, –CH=CH–R2, –CH=C(NO2)–R3, –CH=NOH or –CN, wherein R1 is (C1-10 alkoxycarbonyl; (C1-10 alkoxy)carbonyl monosubstituted by chloro, bromo, cyano, hydroxy, C1-2 alkoxy, (C1-2 alkyl)carbonyloxy or (C1-2 alkoxy)carbonyl; (C1-10 alkoxy)carbonyl disubstituted by hydroxy and by chloro or bromo; (C3-8 alkenyl)oxycarbonyl; (C3-8 chloroalkenyl)oxycarbonyl; (C3-8 bromoalkenyl)oxycarbonyl; propynyloxycarbonyl; benzyloxycarbonyl; chlorobenzyloxycarbonyl; nitrobenzyloxycarbonyl; C1-4 alkylsulfonyl; phenylsulfonyl; tolylsulfonyl; carbamoyl; (C1-2 alkyl)carbamoyl; di(C1-2 alkyl)carbamoyl; phenylcarbamoyl; aminothiocarbonyl; benzimidazolyl-2; cyano; acetyl; phenyl; benzoyl or phenyl or benzoyl substituted by 1, 2 or 3 substituents each of which is independently chloro, bromo or nitro, with the proviso that the maximum number of nitro groups is two, and R2 is phenyl; benzoyl or phenyl or benzoyl substituted by 1, 2 or 3 substituents each of which is independently chloro, bromo or nitro, with the proviso that the maximum number of nitro groups is two, and R3 is hydrogen, methyl or ethyl, and m is 0 or 1, useful as disperse dyes for dyeing and printing textile substrates comprising or consisting of synthetic or semi-synthetic, hydrophobic, high molecular weight, organic materials such as linear aromatic polyesters, cellulose 21/2 acetate, cellulose triacetate and synthetic polyamides, with those wherein R is formyl also being useful for dyeing wool.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.name: 2-Amino-4-chlorothiazole-5-carbaldehyde, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 76874-79-8, in my other articles.
Reference：
Thiazole | C3H1927NS – PubChem,
Thiazole | chemical compound | Britannica