Final Thoughts on Chemistry for 2-Bromobenzothiazole

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.name: 2-Bromobenzothiazole, you can also check out more blogs about2516-40-7

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2516-40-7, Name is 2-Bromobenzothiazole, molecular formula is C7H4BrNS. In a Article,once mentioned of 2516-40-7, Computed Properties of C7H4BrNS

A simple and efficient protocol for the copper-catalyzed synthesis of aryl or alkyl 2,2,2-trifluoroethyl selenoethers has been developed. This reaction proceeded smoothly in the presence of CuI/phen as the catalyst, with elemental selenium, 1,1,1-trifluoro-2-iodoethane, and NaBH4 as reagents in DMF with a broad scope of functionalized (hetero)aryl or alkyl halides. Different functional groups were tolerated and moderate to excellent yields of 2,2,2-trifluoroethyl selenoethers were obtained. Some of the synthesized compounds exhibited promising insecticidal activities.

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.name: 2-Bromobenzothiazole, you can also check out more blogs about2516-40-7

Reference:
Thiazole | C3H2743NS – PubChem,
Thiazole | chemical compound | Britannica