The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2942-13-4, Name is 6-Methoxybenzo[d]thiazole, molecular formula is C8H7NOS. In a Patent£¬once mentioned of 2942-13-4, Recommanded Product: 6-Methoxybenzo[d]thiazole
The invention discloses a substituted benzo thiazole C2 alkylation derivative and its application, the structural formula of the compound of formula (I) as shown: Formula (I) in, benzothiazole ring substituent R is H1 Mono-substituted, multi-substituted or not substituted; n is 0 – 4 of the integer, n said benzothiazole ring substituent R1 The number of; n=0 when, said of the benzothiazole ring H is not substituted; n=1 when, said benzothiazole ring substituent R is H1 Mono-substituted; n=2 – 4 when, said benzothiazole ring substituent R is H1 Multi-substituted, different substituted position substituent on R1 The same or different; the substituent R1 Is hydrogen, C1 – C3 alkyl, C1 – C2 alkoxy, aryl or halogen; formula (I) substituent R2 Is hydrogen or C1 – C3 alkyl. The present invention provides substituted benzothiazole C2 alkylation derivatives, exhibit better bacteriostatic activity, in particular against the dry silk nuclear fungus and exhibits a strong inhibiting activity. (by machine translation)
The invention discloses a substituted benzo thiazole C2 alkylation derivative and its application, the structural formula of the compound of formula (I) as shown: Formula (I) in, benzothiazole ring substituent R is H1 Mono-substituted, multi-substituted or not substituted; n is 0 – 4 of the integer, n said benzothiazole ring substituent R1 The number of; n=0 when, said of the benzothiazole ring H is not substituted; n=1 when, said benzothiazole ring substituent R is H1 Mono-substituted; n=2 – 4 when, said benzothiazole ring substituent R is H1 Multi-substituted, different substituted position substituent on R1 The same or different; the substituent R1 Is hydrogen, C1 – C3 alkyl, C1 – C2 alkoxy, aryl or halogen; formula (I) substituent R2 Is hydrogen or C1 – C3 alkyl. The present invention provides substituted benzothiazole C2 alkylation derivatives, exhibit better bacteriostatic activity, in particular against the dry silk nuclear fungus and exhibits a strong inhibiting activity. (by machine translation)
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.Recommanded Product: 6-Methoxybenzo[d]thiazole, you can also check out more blogs about2942-13-4
Reference£º
Thiazole | C3H7153NS – PubChem,
Thiazole | chemical compound | Britannica