Extended knowledge of 5-(Trifluoromethyl)benzo[d]oxazole

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 1267217-46-8

Application of 1267217-46-8, Because a catalyst decreases the height of the energy barrier, its presence increases the reaction rates of both the forward and the reverse reactions by the same amount.1267217-46-8, Name is 5-(Trifluoromethyl)benzo[d]oxazole, molecular formula is C8H4F3NO. In a article£¬once mentioned of 1267217-46-8

Palladium-catalyzed direct arylation of benzoxazoles with unactivated simple arenes

Using CuBr2 as an additive, the Pd-catalyzed intermolecular C-H-C-H cross-coupling between benzoxazoles and unactivated simple arenes has been developed. This protocol provides a straightforward approach for the biological activity of 2-arylbenzoxazole derivatives.

A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 1267217-46-8

Reference£º
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem