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. 16311-69-6, Name is 5-(2-Hydroxyethyl)-3,4-dimethylthiazol-3-ium iodide, molecular formula is C7H12INOS. In a Article，once mentioned of 16311-69-6, Safety of 5-(2-Hydroxyethyl)-3,4-dimethylthiazol-3-ium iodide
A series of new lipid-like thiazole derivatives have been synthesized in good yields by O-alkylation of 5-(2-hydroxyethyl)-4-methyl-1,3-thiazole, a thiamine metabolite, under phase transfer catalysis conditions followed by N-alkylation with the aim to obtain potential anticancer and antimicrobial agents. The synthesized cationic amphiphiles and their ether precursors were subjected to in vitro cytotoxic evaluation against monolayer human fibrosarcoma HT-1080 and mouse hepatoma MG-22A tumour cell lines and normal mouse NIH 3T3 fibroblasts and were screened for antimicrobial activity concerning gram-positive and gram-negative bacterial and fungal strains. The synthesized compounds possessed strong antimicrobial activity, significant selective cytotoxicity and high NO-induction ability. In vivo investigation of 3,4-dimethyl-5-(2-undecyloxyethyl)-1,3-thiazol-3-ium iodide confirmed anticancer action, reliably inhibiting mouse sarcoma S-180 tumour growth.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Safety of 5-(2-Hydroxyethyl)-3,4-dimethylthiazol-3-ium iodide. In my other articles, you can also check out more blogs about 16311-69-6
Reference：
Thiazole | C3H5952NS – PubChem,
Thiazole | chemical compound | Britannica