Related Products of 14959-32-1, 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.14959-32-1, Name is 3-Chloro-6-(methylamino)pyridazine, molecular formula is C5H6ClN3. In a article，once mentioned of 14959-32-1
Synthesis and properties of mesoionic pyrimido[1,2 b]pyridazine 2,4 diones and mesoionic pyridazino[2,3 a] s triazine 2,4 diones: mesoionic analogs structurally related to fervenulin
Derivatives of two new and unusual classes of heterocycles, possessing structural similarities to the broad spectrum antibiotic fervenulin, were synthesized and examined for in vitro antimicrobial activity. Only three of 17 mesoionic pyrimido[1,2 b]pyridazine 2,4 diones exhibited evidence of antimicrobial activity while seven of eight mesoionic pyridazino[2,3 a]s triazine 2,4 diones were active against one or more microorganisms. Susceptibility toward attack by nucleophiles of both mesoionic pyridazino[2,3 a]s triazine 2,4 diones and fervenulin was observed.
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 14959-32-1
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N1028 – PubChem