Extracurricular laboratory:new discovery of 54109-03-4

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 54109-03-4

Application of 54109-03-4, 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.54109-03-4, Name is 5-Chloroisobenzofuran-1(3H)-one, molecular formula is C8H5ClO2. In a article£¬once mentioned of 54109-03-4

N-Arylation of heterocycles promoted by tetraethylenepentamine in water

Tetraethylenepentamine and triethylenetetramine are found to be efficient organic bases for the N-arylation of pyrazole and imidazole with aryl and heteroaryl-iodides and -bromides catalyzed by CuI in water at moderate temperature. The cross-couplings proceed smoothly with good to excellent yields and a variety of functional groups are tolerated under this condition.

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 54109-03-4

Reference£º
Benzofuran – Wikipedia,
Benzofuran | C8H2646O – PubChem