4-(5-Pyrimidyl)-piperidine is a chemical compound characterized by its piperidine ring, which is a six-membered saturated heterocyclic amine, substituted with a pyrimidine moiety. The pyrimidine ring, a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3, contributes to the compound's potential biological activity. This compound typically exhibits properties such as moderate solubility in polar solvents, which can be influenced by the presence of the nitrogen atoms in both the piperidine and pyrimidine rings. It may also display basicity due to the amine functional group, allowing it to participate in protonation reactions. The structural features of 4-(5-pyrimidyl)-piperidine suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. Its specific interactions with biological targets would depend on the precise arrangement of substituents and the overall three-dimensional conformation of the molecule. As with many heterocyclic compounds, it may also exhibit unique reactivity patterns in organic synthesis.

4-(5-pyrimidyl)-piperidine

733738-49-3: 4-(5-Pyrimidyl)-piperidine is a chemical compound characterized by its piperidine ring, which is a six-membered saturated heterocyclic amine, substituted with a pyrimidine moiety. The pyrimidine ring, a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3, contributes to the compound's potential biological activity. This compound typically exhibits properties such as moderate solubility in polar solvents, which can be influenced by the presence of the nitrogen atoms in both the piperidine and pyrimidine rings. It may also display basicity due to the amine functional group, allowing it to participate in protonation reactions. The structural features of 4-(5-pyrimidyl)-piperidine suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals targeting various biological pathways. Its specific interactions with biological targets would depend on the precise arrangement of substituents and the overall three-dimensional conformation of the molecule. As with many heterocyclic compounds, it may also exhibit unique reactivity patterns in organic synthesis.

CAS 733738-49-3

4-(5-pyrimidyl)-piperidine

5-(Piperidin-4-yl)pyrimidine

Ref: 3D-IEB73849