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. Computed Properties of 3032-92-6.
Shao, Chukai;He, Ying;Yin, Hongquan;Chen, Fu-Xue research published 《 Me3SiCl-Catalyzed Electrophilic Thiocyanation/Cyclization of Alkynylbenzoates to Synthesize 4-Thiocyanatoisocourmarins》, the research content is summarized as follows. A metal-free and regioselective electrophilic thiocyanation/cyclization of alkynylbenzoates was developed to afford series of thiocyanato-containing isocourmarins catalyzed by Me3SiCl. Tandem thiocyanation/6-endo cyclization of alkynylbenzoates was achieved using N-thiocyanatosuccinimide (NTS). A wide scope of substrates and functional groups was tolerated with moderate to excellent yield up to 98%. The mild reaction conditions made this protocol more practical to access isocourmarins bearing a thiocyanato group with diversed transformations.
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%., Computed Properties of 3032-92-6
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts