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Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of 4,5-Dichloro-2-phenylpyridazin-3(2H)-one, you can also check out more blogs about1698-53-9

Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments. Application In Synthesis of 4,5-Dichloro-2-phenylpyridazin-3(2H)-one. Introducing a new discovery about 1698-53-9, Name is 4,5-Dichloro-2-phenylpyridazin-3(2H)-one

A variety of substituted pyridazin-3(2H)-ones are directly N-arylated in good yield using lead tetraacetate/zinc chloride in benzene or in substituted benzenes including chloro- and bromobenzene. A variety of substituted pyridazin-3(2H)-ones are directly N-arylated in good yield using lead tetraacetate/zinc chloride in benzene or in substituted benzenes including chloro- and bromobenzene.

Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Application In Synthesis of 4,5-Dichloro-2-phenylpyridazin-3(2H)-one, you can also check out more blogs about1698-53-9

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N3100 – PubChem