A new application about 5-Bromo-2-mercaptobenzothiazole

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: 5-Bromo-2-mercaptobenzothiazole, you can also check out more blogs about71216-20-1

The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.71216-20-1, Name is 5-Bromo-2-mercaptobenzothiazole, molecular formula is C7H4BrNS2. In a Article，once mentioned of 71216-20-1, Recommanded Product: 5-Bromo-2-mercaptobenzothiazole

Here, we report a chiral copper(II)-bisoxazoline-catalyzed enantioselective ring opening of cyclic diaryliodonium salts with heteroaryl thiols. The readily available 2-mercaptobenzoxazole and 2-mercaptobenzothiazole derivatives reacted efficiently with cyclic diaryliodonium salts and afforded various axially chiral biaryls bearing iodine and sulfur functional groups in excellent yields and enantioselectivities. The products were further transformed into diverse enantiopure alkyl biaryl sulfides, which can be employed as chiral ligands.

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: 5-Bromo-2-mercaptobenzothiazole, you can also check out more blogs about71216-20-1

Reference：
Thiazole | C3H6060NS – PubChem,
Thiazole | chemical compound | Britannica