Application of 4578-58-9, A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 4578-58-9, Name is 6-Methyl-2-phenyl-4,5-dihydropyridazin-3(2H)-one, molecular formula is C11H12N2O. In a Article，once mentioned of 4578-58-9
A General Synthesis of Substituted Indoles from Cyclic Enol Ethers and Enol Lactones
(Equation presented) A general method was developed for the one-pot synthesis of highly functionalized indoles from simple, commercially available aryl hydrazines and cyclic enol ethers. Enol lactones were also used as substrates, affording substituted indole acetic acid or indole propionic acid derivatives. This procedure affords 2,3-disubstituted indoles as single regioisomers from the appropriately substituted enol ether or enol lactone. This method was highlighted in the efficient synthesis of the antimigraine drug sumitriptan and the antiinflammatory drug indomethacin.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Application of 4578-58-9. In my other articles, you can also check out more blogs about 4578-58-9
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2539 – PubChem