Extended knowledge of 50850-93-6

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.Application In Synthesis of Ethyl 2-aminobenzo[d]thiazole-6-carboxylate, you can also check out more blogs about50850-93-6

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.50850-93-6, Name is Ethyl 2-aminobenzo[d]thiazole-6-carboxylate, molecular formula is C10H10N2O2S. In a Article,once mentioned of 50850-93-6, Application In Synthesis of Ethyl 2-aminobenzo[d]thiazole-6-carboxylate

In the current study aimed to investigate a number of heterocyclic compounds 4-amino benzoate (procaine) (A1), where the ester was synthesized by esterification of 4-amino benzoic acid with ethanol. Then, this compound was treated with potassium thiocyanate, followed by oxidative cyclization of the produced thiourea with bromine solution to afford ethyl-2-aminobenzothiazole-6-carboxylate (A2). The produced compound was further treated with some substituted benzaldehyde yielding the Schiff bases (A3a-d). Compound (A2) was also treated with acetic anhydride giving the corresponding N-(ethyl-2-amino benzo thiazolyl-6-carboxylate acetamide (A4). Compound (A4) was allowed to react with hydrazine hydrate afforded 2- benzothiazolyl-6- hydrazido acetamide (A5),which was then condensed with substituted aromatic aldehydes affording 6-[(arylidine hydrazino)-carbonyl]-2-acetamidobenzothiazole as a final product (A6a-d). All the synthesized compounds were characterized by the Infrared (FT-IR) technology. Some of the studied samples were checked by either their elemental analysis, (CHNS), 1H-NMR method, and biological evaluations antibacterial activities for some of the synthesized imides were evaluated against four types of bacteria and in addition to systematic identification of some actives functional groups in these compounds.

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 Ethyl 2-aminobenzo[d]thiazole-6-carboxylate, you can also check out more blogs about50850-93-6

Reference:
Thiazole | C3H10663NS – PubChem,
Thiazole | chemical compound | Britannica