CAS 78165-07-8

Cyclohexanol, 4-phenyl-4-(1-piperidinyl)-, trans-

Description:

Cyclohexanol, 4-phenyl-4-(1-piperidinyl)-, trans- is an organic compound characterized by its cyclohexanol backbone, which features a phenyl group and a piperidine substituent. This compound typically exhibits a colorless to pale yellow appearance and is soluble in organic solvents. The presence of the piperidine ring contributes to its potential biological activity, making it of interest in medicinal chemistry. The trans configuration indicates that the substituents on the cyclohexanol ring are positioned opposite each other, which can influence the compound's spatial orientation and reactivity. Cyclohexanol derivatives often display properties such as moderate volatility and varying degrees of hydrophilicity, depending on the substituents. This compound may also participate in hydrogen bonding due to the hydroxyl group, affecting its physical properties and interactions with other molecules. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if ingested or inhaled.

Formula: C₁₇H₂₅NO

Trans-4-phenyl-4-piperidinocyclohexanol

Controlled Product

CAS: 78165-07-8

Trans-4-phenyl-4-piperidinocyclohexanol (TPC) is an analog of the neurotransmitter dopamine. It has been used as a model compound to study the effects of dopamine on blood pressure and locomotor activity in rats. TPC binds to nicotinic acetylcholine receptors and inhibits the uptake of dopamine by these receptors, leading to hyperlocomotion. TPC also has an inhibitory effect on cyclohexane ring assays and drug metabolites, which may be due to its ability to compete with other drugs for binding sites on plasma proteins. In addition, TPC is actively metabolized by rat striatal cells into various compounds that have not been identified yet.

Formula: C₁₇H₂₅NO

Purity: Min. 95%

Molecular weight: 259.4 g/mol

Ref: 3D-DDA16507