Synthetic Route of 14161-11-6, 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. 14161-11-6, Name is 3,4,5-Trichloropyridazine, molecular formula is C4HCl3N2. In a Article，once mentioned of 14161-11-6
A new quinoxaline 1,4-dioxide benzylsulfanyl derivative was tested under mild conditions in copper-mediated Liebeskind-Srogl (LS) cross-coupling reactions with arene boronic acids. These first organometallic cross-coupling reactions performed on a quinoxaline 1,4-dioxide derivative open new perspectives in medicinal chemistry. They represent also the first LS cross-couplings run with an electrophile equipped with an aryl N-oxide moiety. A mild an efficient protocol was developed to prepare quinoxaline 1,4-dioxide derivatives. A benzylsulfanyl quinoxaline 1,4-dioxide derivative was engaged as an electrophilic partner in copper-mediated Liebeskind-Srogl cross-coupling reactions with a wide range of arene boronic acids. These experiments represent the first organometallic coupling reactions on quinoxaline 1,4-dioxide derivatives. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Synthetic Route of 14161-11-6. In my other articles, you can also check out more blogs about 14161-11-6
Reference：
Pyridazine – Wikipedia,
Pyridazine | C4H4N2501 – PubChem