Industrially, the main methods for producing nitriles are ammoxidation and hydrocyanation. 20099-89-2, formula is C9H6BrNO, Name is 4-(2-Bromoacetyl)benzonitrile. Both routes are green in the sense that they do not generate stoichiometric amounts of salts. COA of Formula: C9H6BrNO.
Samanta, Apurba;Pramanik, Shyamal;Mondal, Subhashis;Maity, Soumitra research published 《 Zinc acetate-promoted blocking of the ATRA process with alkyl halides enabling photochemical alkylamination of olefins》, the research content is summarized as follows. Organic photoredox-catalyzed alkylamination of olefins was performed with alkyl halides and nitrile solvent by blocking the traditional photoredox-ATRA process with Zn(OAc)2. A range of carbon-centered radicals (α-alkylcarbonyl, benzyl, cyanomethyl) were effectively participating in this strategy giving rise to versatile carboamination products with high synthetic value.
COA of Formula: C9H6BrNO, 4-(2-Bromoacetyl)benzonitrile, also known as 2-Bromo-4′ -cyanoacetophenone, is a useful research compound. Its molecular formula is C9H6BrNO and its molecular weight is 224.05 g/mol. The purity is usually 95%.
2-Bromo-4′ -cyanoacetophenone can be synthesized from ethylbenzene via aerobic photooxidation using aqueous HBr.
4-(2-Bromoacetyl)benzonitrile is useful for the irreversible inhibitory activity of Glycogen synthase kinase 3 (GSK-3). Phenylhalomethylketones can be used in the study of novel GSK-3 inhibitors., 20099-89-2.
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts