Kamogawa, Hiroyoshi et al. published their research in Bulletin of the Chemical Society of Japan in 1983 | CAS: 4435-14-7

2-Cyclohexylacetonitrile (cas: 4435-14-7) belongs to nitriles. Trimerization of aromatic nitriles requires harsh reaction conditions, high temperatures, long reaction times, and pressure. Nitrile groups in organic compounds can undergo a variety of reactions depending on the reactants or conditions. A nitrile group can be hydrolyzed, reduced, or ejected from a molecule as a cyanide ion.Name: 2-Cyclohexylacetonitrile

Conversions of carbonyl compounds via their polymeric sulfonylhydrazones into alkenes, alkanes, and nitriles was written by Kamogawa, Hiroyoshi;Kanzawa, Asami;Kadoya, Masahiro;Naito, Takeshi;Nanasawa, Masato. And the article was included in Bulletin of the Chemical Society of Japan in 1983.Name: 2-Cyclohexylacetonitrile This article mentions the following:

RR1CO [R = H, R1 = (CH2)5Me, Ph, cyclohexyl; R = Me, R1 = Ph, CH2CH2Ph; R = R1 = Ph, CH2Ph; RR1 = (CH2)5, (CH2)11, (CH2)2CHMe; RR1CO = camphor] reacted with hydrazine bound to sulfonated styrene-divinylbenzene copolymer to form polymer-bound sulfonylhydrazones (I). I reacted with alkali to give alkenes, with NaBH4 or LiAlH4 to give RCHiR1, and with KCN to give RR1CHCN. The extent of the reaction depended on the type of resin and the bulk of RR1CO. 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. Trimerization of aromatic nitriles requires harsh reaction conditions, high temperatures, long reaction times, and pressure. Nitrile groups in organic compounds can undergo a variety of reactions depending on the reactants or conditions. A nitrile group can be hydrolyzed, reduced, or ejected from a molecule as a cyanide ion.Name: 2-Cyclohexylacetonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts