Synthesis of some (nitropyridyl)acetonitriles was written by Katz, R. B.;Voyle, M.. And the article was included in Synthesis in 1989.HPLC of Formula: 123846-66-2 This article mentions the following:
Reaction of chloronitropyridines, e.g., I (R = Cl, R1 = H; R = H, R1 = Cl), with NCCH2CO2CMe3 in THF containing K2CO3 gave cyano(nitropyridyl)acetates, e.g., I [R = CH(CN)CO2CMe3, R1 = H; R = H, R1 = CH(CN)CO2CMe3]. Isolation and decarboxylation or in situ decarboxylation by treatment with p-MeC6H4SO3H in PhMe gave the title compounds in some cases, e.g., I (R = CH2CN, R1 = H). In the experiment, the researchers used many compounds, for example, 2-(5-Nitro-2-pyridinyl)acetonitrile (cas: 123846-66-2HPLC of Formula: 123846-66-2).
2-(5-Nitro-2-pyridinyl)acetonitrile (cas: 123846-66-2) belongs to nitriles. There has been no report on the microbial biosynthesis of nitriles and the physiological function of such enzymes, nor was it not even known whether aliphatic and aromatic nitriles are biological compounds or just petrochemicals. Some nitriles are manufactured by heating carboxylic acids with ammonia in the presence of catalysts. This process is used to make nitriles from natural fats and oils, the products being used as softening agents in synthetic rubbers, plastics, and textiles and for making amines.HPLC of Formula: 123846-66-2
Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts