(R)-(+)-Alpha-(3-hydroxy-2-methoxyphenyl)-1-[2-(4-fluoro-phenyl)ethyl]-4-piperidine methanol, with CAS number 189192-18-5, is a chemical compound characterized by its complex structure, which includes a piperidine ring and various functional groups such as hydroxyl, methoxy, and fluorophenyl moieties. This compound is typically classified as a piperidine derivative and may exhibit properties relevant to pharmacology, particularly in the context of central nervous system activity. The presence of the hydroxyl and methoxy groups suggests potential for hydrogen bonding and lipophilicity, which can influence its solubility and bioavailability. The fluorophenyl group may enhance the compound's potency or selectivity for specific biological targets. As with many synthetic organic compounds, its stereochemistry is crucial for its biological activity, with the (R)-enantiomer often being the active form. Overall, this compound's unique structural features may contribute to its potential applications in medicinal chemistry and drug development.

(R)-(+)-ALPHA-(3-HYDROXY-2-METHOXYPHENYL)-1-[2-(4-FLUORO-PHENYL)ETHYL]-4-PIPERIDINE METHANOL

189192-18-5: (R)-(+)-Alpha-(3-hydroxy-2-methoxyphenyl)-1-[2-(4-fluoro-phenyl)ethyl]-4-piperidine methanol, with CAS number 189192-18-5, is a chemical compound characterized by its complex structure, which includes a piperidine ring and various functional groups such as hydroxyl, methoxy, and fluorophenyl moieties. This compound is typically classified as a piperidine derivative and may exhibit properties relevant to pharmacology, particularly in the context of central nervous system activity. The presence of the hydroxyl and methoxy groups suggests potential for hydrogen bonding and lipophilicity, which can influence its solubility and bioavailability. The fluorophenyl group may enhance the compound's potency or selectivity for specific biological targets. As with many synthetic organic compounds, its stereochemistry is crucial for its biological activity, with the (R)-enantiomer often being the active form. Overall, this compound's unique structural features may contribute to its potential applications in medicinal chemistry and drug development.

CAS 189192-18-5

(R)-(+)-ALPHA-(3-HYDROXY-2-METHOXYPHENYL)-1-[2-(4-FLUORO-PHENYL)ETHYL]-4-PIPERIDINE METHANOL