A new application about 20358-03-6

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.Quality Control of: 2-Amino-5-bromobenzothiazole, you can also check out more blogs about20358-03-6

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.20358-03-6, Name is 2-Amino-5-bromobenzothiazole, molecular formula is C7H5BrN2S. In a Article,once mentioned of 20358-03-6, Quality Control of: 2-Amino-5-bromobenzothiazole

Metal-free oxidative cyclization for the one-pot synthesis of benzo[d]imidazo[2,1-b]thiazoles from 2-aminobenzothiazoles and cyclic ketones is described. Elemental sulfur combined with molecular oxygen as the benign co-oxidant was found to be unique and highly effective to promote this transformation without the aid of any metal salts. Various cyclic ketones smoothly reacted with 2-aminobenzothiazoles to give functional benzo[d]imidazo[2,1-b]thiazoles in good to very high yields, which thereby demonstrated the synthetic convergence of this methodology.

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.Quality Control of: 2-Amino-5-bromobenzothiazole, you can also check out more blogs about20358-03-6

Reference:
Thiazole | C3H2049NS – PubChem,
Thiazole | chemical compound | Britannica