Frutos, Rogelio P. et al. published their research in Journal of Organic Chemistry in 2013 | CAS: 62718-31-4

1-Benzylpiperidine-4-carbonitrile (cas: 62718-31-4) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N–H bond in an axial position, and the other in an equatorial position.Computed Properties of C13H16N2

One-Pot Synthesis of 2,5-Disubstituted Pyrimidines from Nitriles was written by Frutos, Rogelio P.;Wei, Xudong;Patel, Nitinchandra D.;Tampone, Thomas G.;Mulder, Jason A.;Busacca, Carl A.;Senanayake, Chris H.. And the article was included in Journal of Organic Chemistry in 2013.Computed Properties of C13H16N2 This article mentions the following:

A practical, one-step process for the synthesis of 2,5-disubstituted pyrimidines is presented. The protocol proved to be general for the synthesis of a variety of pyrimidine-containing compounds bearing an assortment of functional groups. In the experiment, the researchers used many compounds, for example, 1-Benzylpiperidine-4-carbonitrile (cas: 62718-31-4Computed Properties of C13H16N2).

1-Benzylpiperidine-4-carbonitrile (cas: 62718-31-4) belongs to piperidine derivatives. Piperidine has a role as a reagent, a protic solvent, a base, a catalyst, a plant metabolite, a human metabolite and a non-polar solvent. Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N–H bond in an axial position, and the other in an equatorial position.Computed Properties of C13H16N2

Referemce:
Piperidine – Wikipedia,
Piperidine | C5H11N – PubChem