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CAS 176022-03-0

:

3S,4R-4-[phenyl-1-methylpiperidinyl] methanol

Description:
3S,4R-4-[phenyl-1-methylpiperidinyl] methanol, with the CAS number 176022-03-0, is a chemical compound characterized by its specific stereochemistry, indicated by the 3S and 4R configuration. This compound features a piperidine ring substituted with a phenyl group and a methyl group, contributing to its potential biological activity. The presence of the hydroxymethyl group (-CH2OH) suggests that it may exhibit properties typical of alcohols, such as solubility in polar solvents and the ability to participate in hydrogen bonding. The stereochemical configuration is crucial for its interaction with biological targets, potentially influencing its pharmacological profile. Compounds with similar structures are often investigated for their effects on the central nervous system, given the piperidine moiety's prevalence in psychoactive substances. Overall, the unique combination of its functional groups and stereochemistry may confer specific reactivity and biological properties, making it a subject of interest in medicinal chemistry and drug development.
Formula:C13H19NO
Synonyms:
  • (3S,4R)-1-methyl-4-phenyl-3-Piperidinemethanol
  • [(3S,4R)-4-Phenyl-1-methylpiperidinyl]methanol,99%e.e.
  • 3S,4R-4-[phenyl-1-methylpiperidinyl] methanol
  • Paroxetine Impurity 21
  • 3-Piperidinemethanol, 1-methyl-4-phenyl-, (3S,4R)-
  • Paroxetine Impurity 7
  • Paroxetine impurities798
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