Application In Synthesis of 6-Chloro-3-hydroxypyridazine, The prevalence of solvent effects in heterogeneous catalysis in condensed media has motivated developing quantitative kinetic and theoretical assessments of solvent structures and their interactions with reaction intermediates and transition states.
Electrochemical reduction of 3-chloropyridazine derivatives in DMF involves cleavage of the C-Cl bond as the initial stage. In the case of 3-chloro-6-(2-benzylidene-1-methylhydrazino)pyridazine, elimination of the chloride ion is followed by cleavage of the N-N bond in the hydrazone moiety (amino-nitrile cleavage).
I am very proud of our efforts over the past few months and hope to 19064-67-6 help many people in the next few years.Application In Synthesis of 6-Chloro-3-hydroxypyridazine
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N762 – PubChem