4-(4-Chloro-phenylsulfanyl)-piperidine, identified by its CAS number 101768-63-2, is a chemical compound characterized by its piperidine core, which is a six-membered saturated heterocyclic ring containing one nitrogen atom. The presence of a 4-chlorophenylsulfanyl group indicates that a chlorinated phenyl group is attached to a sulfur atom, which is further linked to the piperidine ring. This compound exhibits properties typical of piperidine derivatives, including potential applications in medicinal chemistry due to its ability to interact with biological targets. The chlorinated phenyl group may enhance lipophilicity and influence the compound's pharmacokinetic properties. Additionally, the sulfur atom can participate in various chemical reactions, making this compound of interest in synthetic organic chemistry. Its specific characteristics, such as solubility, melting point, and reactivity, would depend on the molecular interactions and the environment in which it is studied. Overall, 4-(4-chloro-phenylsulfanyl)-piperidine represents a versatile structure with potential implications in drug development and chemical synthesis.

4-(4-CHLORO-PHENYLSULFANYL)-PIPERIDINE

101768-63-2: 4-(4-Chloro-phenylsulfanyl)-piperidine, identified by its CAS number 101768-63-2, is a chemical compound characterized by its piperidine core, which is a six-membered saturated heterocyclic ring containing one nitrogen atom. The presence of a 4-chlorophenylsulfanyl group indicates that a chlorinated phenyl group is attached to a sulfur atom, which is further linked to the piperidine ring. This compound exhibits properties typical of piperidine derivatives, including potential applications in medicinal chemistry due to its ability to interact with biological targets. The chlorinated phenyl group may enhance lipophilicity and influence the compound's pharmacokinetic properties. Additionally, the sulfur atom can participate in various chemical reactions, making this compound of interest in synthetic organic chemistry. Its specific characteristics, such as solubility, melting point, and reactivity, would depend on the molecular interactions and the environment in which it is studied. Overall, 4-(4-chloro-phenylsulfanyl)-piperidine represents a versatile structure with potential implications in drug development and chemical synthesis.

CAS 101768-63-2

4-(4-CHLORO-PHENYLSULFANYL)-PIPERIDINE

4-[(4-Chlorophenyl)sulfanyl]piperidine

Ref: IN-DA0005F6