1-(4-Chlorophenyl)piperidin-4-amine, identified by its CAS number 897652-03-8, is a chemical compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. The presence of a 4-chlorophenyl group indicates that a chlorine atom is substituted on the phenyl ring at the para position, which can influence the compound's biological activity and lipophilicity. This compound is typically classified as an amine due to the presence of the amine functional group (-NH2) attached to the piperidine ring. It may exhibit properties such as being a potential pharmacological agent, with applications in medicinal chemistry, particularly in the development of drugs targeting various neurological or psychiatric conditions. The structural features of 1-(4-chlorophenyl)piperidin-4-amine suggest it may interact with neurotransmitter systems, although specific biological activities would depend on further empirical studies. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups.

1-(4-CHLOROPHENYL)PIPERIDIN-4-AMINE

897652-03-8: 1-(4-Chlorophenyl)piperidin-4-amine, identified by its CAS number 897652-03-8, is a chemical compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. The presence of a 4-chlorophenyl group indicates that a chlorine atom is substituted on the phenyl ring at the para position, which can influence the compound's biological activity and lipophilicity. This compound is typically classified as an amine due to the presence of the amine functional group (-NH2) attached to the piperidine ring. It may exhibit properties such as being a potential pharmacological agent, with applications in medicinal chemistry, particularly in the development of drugs targeting various neurological or psychiatric conditions. The structural features of 1-(4-chlorophenyl)piperidin-4-amine suggest it may interact with neurotransmitter systems, although specific biological activities would depend on further empirical studies. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups.

CAS 897652-03-8

1-(4-CHLOROPHENYL)PIPERIDIN-4-AMINE