Brief introduction of 3,6-Dichloropyridazine

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 141-30-0

Electric Literature of 141-30-0, 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.141-30-0, Name is 3,6-Dichloropyridazine, molecular formula is C4H2Cl2N2. In a article,once mentioned of 141-30-0

On the basis of ideas recently advanced regarding the origin of enantioselectivity in the OsO4 promoted dihydroxylation of olefins catalyzed by bis-cinchona alkaloid derivatives such as 1, specifically strong evidence for reaction via transition state assembly 2, the mono-quinidine derivative 3 was selected as a promising catalytic ligand.The experimental observation of high enantioselectivity promoted by 3 provides additional evidence in favor of transition-state 2.

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 141-30-0

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N1657 – PubChem