Final Thoughts on Chemistry for 20358-00-3

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.Application In Synthesis of 2-Amino-5-chlorobenzothiazole, you can also check out more blogs about20358-00-3

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.20358-00-3, Name is 2-Amino-5-chlorobenzothiazole, molecular formula is C7H5ClN2S. In a Article，once mentioned of 20358-00-3, Application In Synthesis of 2-Amino-5-chlorobenzothiazole

VILSMEIER-HAACK REACTION OF 2-AMINO-X-BENZOTHIAZOLES WITH N-PHENYLFORMAMIDE IN THE PRESENCE OF BENZENESULFONYL CHLORIDE

2-Amino-X-benzothiazoles (X = H, 4-Cl, 6-Cl, 6-NO2, 6-CH3, 6-OCH3, 6-Br) react with N-phenylformamide and two equivalents of benzenesulfonyl chloride in pyridine, affording different products in dependence on the substituent X: N-(X-2-benzothiazolyl)formamidines, N-phenyl-N’-(X-2-benzothiazolyl)formamidines, N-phenyl-N’,N”-bis(X-2-benzothiazolyl)triaminomethanes, N-(X-2-benzothiazolyl)benzenesulfonamides and N-2-((X-3-phenyliminomethyl)benzothiazolylidene)benzenesulfonamides.In the presence of one equivalent of benzenesulfonyl chloride, benzothiazoles I either do not react or are partially benzenesulfonated.

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.Application In Synthesis of 2-Amino-5-chlorobenzothiazole, you can also check out more blogs about20358-00-3

Reference：
Thiazole | C3H2183NS – PubChem,
Thiazole | chemical compound | Britannica