Extended knowledge of 2-(4-Methylphenyl)benzothiazole

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.Safety of 2-(4-Methylphenyl)benzothiazole, you can also check out more blogs about16112-21-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.16112-21-3, Name is 2-(4-Methylphenyl)benzothiazole, molecular formula is C14H11NS. In a Article，once mentioned of 16112-21-3, Safety of 2-(4-Methylphenyl)benzothiazole

A new strategy for synthesis of imines using the approach of release of H2 has been developed. This oxidant- and acceptor-free Pd/C catalysis protocol is further applied to synthesis of benzoxazoles, benzimidazoles, and benzothiazoles through a one-pot cascade reaction with notably high yields. The Royal Society of Chemistry 2013.

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.Safety of 2-(4-Methylphenyl)benzothiazole, you can also check out more blogs about16112-21-3

Reference：
Thiazole | C3H857NS – PubChem,
Thiazole | chemical compound | Britannica