Application of 22808-29-3, Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps.In a article, 22808-29-3, molcular formula is C8H10Cl2N2, introducing its new discovery.
3,6-Dichloro-4-(2-chloro-1,1-dimethylethyl)pyridazine (3) is a systemic plant fungicide whose synthesis by several routes is described.Free-radical alkylations of 3,6-dichloropyridazine (1) gave either the 4-tert-butyl derivative 2 or the alcohol 3,6-dichloro-beta,beta-dimethyl-4-pyridazineethanol (24).Pyridazine (2) must be subjected to a free-radical chlorination, which resulted in other products, but alcohol 24 could be smoothly converted to 3.Alternatively, the pyridazine ring was constructed with the side chain preattached by utilizing lactone intermediates 10 or 18.The lactone 10 with hydrazine yielded the ether 11, and chlorination with ether cleavage proceeded to 3.Lactone 20 could not be transformed to 3.
The proportionality constant is the rate constant for the particular unimolecular reaction. the reaction rate is directly proportional to the concentration of the reactant. I hope my blog about 22808-29-3 is helpful to your research. Application of 22808-29-3
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2891 – PubChem