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. 79265-30-8, Name is 2-(Trimethylsilyl)thiazole, molecular formula is C6H11NSSi. In a Article，once mentioned of 79265-30-8, Computed Properties of C6H11NSSi
Starting substrates, enantiopure spiranic or 3-substituted 3-alkoxy-4-oxoazetidine-2-carbaldehydes, were prepared from (R)-2,3-O- isopropylideneglyceraldehyde derived azetidine-2,3-diones by sequential Barbier-type addition reactions followed by hydroxy functionalization and aldehyde unmasking. The reaction between the above beta-lactam aldehydes and 2-(trimethylsilyl)thiazole (TMST) gave as major products conformationally constrained alpha-alkoxy-gamma-keto amides, which can be considered both as aldols as well as Passerini-type products, by N1-C4 beta-lactam bond cleavage. Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Computed Properties of C6H11NSSi. In my other articles, you can also check out more blogs about 79265-30-8
Reference：
Thiazole | C3H1085NS – PubChem,
Thiazole | chemical compound | Britannica