A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 23031-78-9, Name is Benzo[d]isothiazol-3-amine, molecular formula is C7H6N2S. In a Patent£¬once mentioned of 23031-78-9, SDS of cas: 23031-78-9
The use in pest control of 3-acrylaminobenzisothiazoles of the formula I STR1 wherein R1 is unsubstituted or substituted alkyl or phenyl, R2, R3, R4 and R5 independently of one another are each hydrogen, halogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, and R6 is hydrogen or –COR1. There are also described the novel compounds of the formula Ia STR2 wherein R1 ‘ is C1 -C10 -alkyl substituted by halogen or by C1 -C5 -alkoxy, or is unsubstituted C2 -C10 -alkyl or phenyl, R2 ‘, R3 ‘, R4 ‘ and R5 ‘ independently of one another are each hydrogen, halogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, and R6 ‘ is hydrogen or –COR1 ‘; or R1 ‘ is methyl, R2 ‘, R3 ‘, R4 ‘ and R5 ‘ independently of one another are each hydrogen, halogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, and R6 ‘ is hydrogen; or R1 ‘ is methyl, R2 ‘ is hydrogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, R3 ‘, R4 ‘ and R5 ‘ independently of one another are each hydrogen, trifluoromethyl, amino or nitro, and R6 ‘ is –COR1 ‘; and also described are pesticidal compositions containing, as active ingredients, compounds of the formulae I and Ia, as well as processes for producing these 2-acylaminobenzisothiazoles.
The use in pest control of 3-acrylaminobenzisothiazoles of the formula I STR1 wherein R1 is unsubstituted or substituted alkyl or phenyl, R2, R3, R4 and R5 independently of one another are each hydrogen, halogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, and R6 is hydrogen or –COR1. There are also described the novel compounds of the formula Ia STR2 wherein R1 ‘ is C1 -C10 -alkyl substituted by halogen or by C1 -C5 -alkoxy, or is unsubstituted C2 -C10 -alkyl or phenyl, R2 ‘, R3 ‘, R4 ‘ and R5 ‘ independently of one another are each hydrogen, halogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, and R6 ‘ is hydrogen or –COR1 ‘; or R1 ‘ is methyl, R2 ‘, R3 ‘, R4 ‘ and R5 ‘ independently of one another are each hydrogen, halogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, and R6 ‘ is hydrogen; or R1 ‘ is methyl, R2 ‘ is hydrogen, C1 -C5 -alkyl, C1 -C5 -alkoxy, trifluoromethyl, amino or nitro, R3 ‘, R4 ‘ and R5 ‘ independently of one another are each hydrogen, trifluoromethyl, amino or nitro, and R6 ‘ is –COR1 ‘; and also described are pesticidal compositions containing, as active ingredients, compounds of the formulae I and Ia, as well as processes for producing these 2-acylaminobenzisothiazoles.
Sometimes chemists are able to propose two or more mechanisms that are consistent with the available data.SDS of cas: 23031-78-9, If a proposed mechanism predicts the wrong experimental rate law, however, the mechanism must be incorrect.Welcome to check out more blogs about 23031-78-9, in my other articles.
Reference£º
Thiazole | C3H7442NS – PubChem,
Thiazole | chemical compound | Britannica