4-(4-Chlorophenyl)piperidine, also known by its CAS number 26905-02-2, is an organic compound characterized by a piperidine ring substituted with a para-chlorophenyl group. This compound typically appears as a white to off-white solid and is known for its role in medicinal chemistry, particularly in the development of psychoactive drugs. Its molecular structure consists of a six-membered piperidine ring, which is a saturated nitrogen-containing heterocycle, and a chlorinated phenyl group that enhances its lipophilicity and biological activity. The presence of the chlorine atom can influence the compound's pharmacological properties, including its binding affinity to various receptors. 4-(4-Chlorophenyl)piperidine may exhibit various biological activities, making it of interest in research related to neuropharmacology and potential therapeutic applications. However, handling this compound requires caution due to its potential toxicity and the need for appropriate safety measures in laboratory settings.

4-(4-Chlorophenyl)piperidine

26905-02-2: Piperidine, 4-(4-chlorophenyl)-, Piperidine, 4-(p-chlorophenyl)-, 4-(4-Chlorophenyl)piperidine

Piperidine, 4-(4-chlorophenyl)-

4-(4-Chlorophenyl)piperidine is a piperidine molecule that is an amine and wake-promoting agent. It has affinity for the serotonin transporter and has been shown to be a potent antagonist of serotonin. 4-(4-Chlorophenyl)piperidine is an isomer of modafinil, which has been shown to optimize cognition, memory, and mood in healthy volunteers. The hydroxyl group on the 4-(4-chlorophenyl)piperidine molecule allows for the interaction with dopamine receptors and may also be responsible for its antidepressant properties.

CAS 26905-02-2: 4-(4-Chlorophenyl)piperidine

Piperidine, 4-(4-chlorophenyl)-

Ref: IN-DA00I53A

4-(4-Chlorophenyl)piperidine

Ref: 54-OR8735

4-(4-Chlorophenyl)piperidine

Ref: 10-F216419

4-(4-Chlorophenyl)piperidine

Ref: 3B-C3337

4-(4-Chlorophenyl)piperidine

Ref: 3D-FC148654