Masuda, Yuzuru et al. published their research in Journal of the Chemical Society, Chemical Communications in 1989 | CAS: 4435-14-7

2-Cyclohexylacetonitrile (cas: 4435-14-7) 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. In addition, Nitriles can react with alkynes, which leads to an increase in carbon chain length (carbocyanation).Name: 2-Cyclohexylacetonitrile

A new facile route to primary alkanenitriles from terminal alkenes via a hydroboration-cyanation sequence was written by Masuda, Yuzuru;Hoshi, Masayuki;Arase, Akira. And the article was included in Journal of the Chemical Society, Chemical Communications in 1989.Name: 2-Cyclohexylacetonitrile This article mentions the following:

Alkenes R1CR2:CH2 (R1 = alkyl, R2 = H or Me) underwent hydroboration with dicyclohexylborane, and treatment of the intermediates with CuCN, Cu(OAc)2, and cupric acetylacetonate gave R1CHR2CH2CN. Methylenecyclopentane of methylenecyclohexane gave the resp. cycloalkaneacetonitriles. In the experiment, the researchers used many compounds, for example, 2-Cyclohexylacetonitrile (cas: 4435-14-7Name: 2-Cyclohexylacetonitrile).

2-Cyclohexylacetonitrile (cas: 4435-14-7) 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. In addition, Nitriles can react with alkynes, which leads to an increase in carbon chain length (carbocyanation).Name: 2-Cyclohexylacetonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts