Application of 62476-58-8, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 62476-58-8, Name is 2-Chloro-3-(trifluoromethyl)aniline, SMILES is NC1=CC=CC(C(F)(F)F)=C1Cl, belongs to isothiazole compound. In a article, author is Yang, XP, introduce new discover of the category.
Syntheses and biological activities of 2-arylamidothioacyl-3-isothiozolones and 4-cyano-5-methylthio-2-arylamidothioacyl-3-isothiozolones
Novel compounds, 8-aryiamidothioacyl-3-isothiozolones 6 and 4-cyano-5-methylthio-2-arylamidothioacyl-3-isothiozolones 7 were synthesized by reacting of 3-hydroxyisothiozoles (4, 5) with aryl isothiocyanates 3, The unique coupling constants of 4-H and 5-H of isothiazole ring of compounds 6 were discovered and explained according to the coplanarity of isothiazole ring with thioacyl group, The preliminary test of fungicidal activity showed that some of the title compounds possessed promising activity.
Application of 62476-58-8, Each elementary reaction can be described in terms of its molecularity, the number of molecules that collide in that step. The slowest step in a reaction mechanism is the rate-determining step.you can also check out more blogs about 62476-58-8.
Reference:
Isothiazole – Wikipedia,
,Isothiazole – ScienceDirect.com