The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.19952-47-7, Name is 2-Amino-4-chlorobenzothiazole, molecular formula is C7H5ClN2S. In a Article£¬once mentioned of 19952-47-7, Application In Synthesis of 2-Amino-4-chlorobenzothiazole
Polarographic and cyclic voltammetric behaviour of twelve titled compounds have been studied in the pH range 2.0-11.2 at dropping mercury electrode, pyrolytic graphite electrode and platinum electrode.The effect of substituents, covering wide range of Hammett substituents constant values, has been evaluated quantitatively.
Polarographic and cyclic voltammetric behaviour of twelve titled compounds have been studied in the pH range 2.0-11.2 at dropping mercury electrode, pyrolytic graphite electrode and platinum electrode.The effect of substituents, covering wide range of Hammett substituents constant values, has been evaluated quantitatively.
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-4-chlorobenzothiazole, you can also check out more blogs about19952-47-7
Reference£º
Thiazole | C3H10011NS – PubChem,
Thiazole | chemical compound | Britannica