3-[(2,4-Dimethylphenoxy)methyl]piperidine is an organic compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. The presence of a 2,4-dimethylphenoxy group attached to the piperidine ring significantly influences its chemical properties and biological activity. This compound typically exhibits moderate to high lipophilicity due to the aromatic ring, which can enhance its ability to cross biological membranes. The dimethyl substitutions on the phenyl ring can affect its steric and electronic properties, potentially influencing interactions with biological targets. Additionally, the piperidine moiety can participate in hydrogen bonding and may serve as a basic site, contributing to its reactivity and potential pharmacological effects. The compound may be of interest in medicinal chemistry for its potential applications in drug development, particularly in areas related to central nervous system activity or as a scaffold for further modifications. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions and the presence of other functional groups.

3-[(2,4-DIMETHYLPHENOXY)METHYL]PIPERIDINE

946713-14-0: 3-[(2,4-Dimethylphenoxy)methyl]piperidine is an organic compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. The presence of a 2,4-dimethylphenoxy group attached to the piperidine ring significantly influences its chemical properties and biological activity. This compound typically exhibits moderate to high lipophilicity due to the aromatic ring, which can enhance its ability to cross biological membranes. The dimethyl substitutions on the phenyl ring can affect its steric and electronic properties, potentially influencing interactions with biological targets. Additionally, the piperidine moiety can participate in hydrogen bonding and may serve as a basic site, contributing to its reactivity and potential pharmacological effects. The compound may be of interest in medicinal chemistry for its potential applications in drug development, particularly in areas related to central nervous system activity or as a scaffold for further modifications. As with many organic compounds, its stability, solubility, and reactivity can vary based on environmental conditions and the presence of other functional groups.

CAS 946713-14-0

3-[(2,4-DIMETHYLPHENOXY)METHYL]PIPERIDINE