Industrially, the main methods for producing nitriles are ammoxidation and hydrocyanation. 3032-92-6, formula is C9H5N, Name is 4-Ethynylbenzonitrile. Both routes are green in the sense that they do not generate stoichiometric amounts of salts. Name: 4-Ethynylbenzonitrile.
Kumar, Manoj;Verma, Shalini;Mishra, Vivek;Reiser, Oliver;Verma, Akhilesh K. research published 《 Visible-light-accelerated copper-catalyzed [3 + 2] cycloaddition of N-tosylcyclopropylamines with alkynes/alkenes》, the research content is summarized as follows. Copper-catalyzed [3 + 2] cycloadditions of N-tosylcyclopropylamine with alkynes and alkenes had been accomplished under visible light irradiation The developed approach was compatible with a range of functionalities and allows the synthesis of diversified aminated cyclopentene I [R = Ph, 4-MeOC6H4, 6-methoxy-2-naphthyl, etc.] and cyclopentane derivatives II [R1 = Ph, 4-MeC6H4, Bz, etc.] being relevant for drug synthesis. The protocol was operationally simple and economically affordable as it does not require any ligand, base or additives. As the key step, the one-electron oxidation of the N-tosyl moiety by visible light-induced homolysis of a transient Cu(II)-tosylamide complex was proposed, providing a facile entry for N-centered radicals.
3032-92-6, 4-Ethynylbenzonitrile is a simple benzyl alkyne compound potentially useful as a synthetic fragment and as a test compound for cross-coupling protocols. 4-Ethynylbenzonitrile has been described as a model compound for studying hydrogen bond formation in multifunctional molecules, as it contains four hydrogen bonding sites of which three are π-acceptors.
4-Ethynylbenzonitrile is a useful research compound. Its molecular formula is C9H5N and its molecular weight is 127.14 g/mol. The purity is usually 95%., Name: 4-Ethynylbenzonitrile
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts