Electric Literature of 19064-67-6, 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.19064-67-6, Name is 6-Chloro-3-hydroxypyridazine, molecular formula is C4H3ClN2O. In a article，once mentioned of 19064-67-6
The synthesis of a new series of heteroaromatic macrocycles 6-9 containing the 1,3-bis(6-oxopyridazin-1-yl)propane and pyridine units is reported. The acyclic compounds 11-15 had to be prepared as the intermediates in the synthetic sequence. Evaluation of the ionophoric properties of 6-9 and 11-15 shows that 8 and 13 behave as good ammonium ion carriers and exhibit a high selectivity for ammonium with respect to spherically symmetric metallic ions like Na+, K+, and Ca2+. Molecular modelling of the ammonium complexes suggests that the host’s oxyimino groups play a more relevant part in effective complexation than the pyridine unit, and that the high complexating efficiency of 13 might be related to the formation of a pseudocavity by intramolecular hydrogen bonding.
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 19064-67-6
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N748 – PubChem