Nitrile is any organic compound with a −C≡N functional group. 20099-89-2, formula is C9H6BrNO, Name is 4-(2-Bromoacetyl)benzonitrile.The prefix cyano- is used interchangeably with the term nitrile in literature. Quality Control of 20099-89-2.
De-Zordo Banliat, Arnaud;Grollier, Kevin;Damond, Aurelie;Billard, Thierry;Dagousset, Guillaume;Magnier, Emmanuel;Pegot, Bruce research published 《 Solvent-free nucleophilic selenocyanation with [bmim][SeCN]. Direct access to perfluoroalkylselenide compounds》, the research content is summarized as follows. Available online-1-n-butyl-3-methylimidazolium selenocyanate ([bmim][SeCN]) proved to be a very efficient reagent for selenocyanation of alkyl halides RBr [R = n-decyl, 6-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)hexyl, 9H-fluoren-9-yl, etc.]. As part of an eco-friendly process, no organic solvents were used during the transformation and reaction times were reduced by using microwave as a heating source. The ionic liquid was carefully recycled in two different ways. Selenocyanate compounds RSeCN were successfully transformed into (trifluoromethyl or polyfluoro)selenides RSeR1 (R1 = CF3, CF2Br, C2F5) in a one-pot two step procedure.
Quality Control of 20099-89-2, 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