3-[(4-Fluorophenoxy)methyl]piperidine is a chemical compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. The presence of a 4-fluorophenoxy group attached to the piperidine at the 3-position contributes to its unique properties. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its moderate polarity. The fluorine atom in the phenoxy group can influence the compound's electronic properties, potentially enhancing its biological activity or altering its interaction with biological targets. 3-[(4-Fluorophenoxy)methyl]piperidine is of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential applications in treating various conditions. Its structure allows for the possibility of forming hydrogen bonds and engaging in π-π interactions, which are crucial for binding to biological receptors. As with many piperidine derivatives, it may exhibit a range of pharmacological activities, making it a subject of research in drug discovery and development.

3-[(4-fluorophenoxy)methyl]piperidine

142220-38-0: 3-[(4-Fluorophenoxy)methyl]piperidine is a chemical compound characterized by its piperidine core, which is a six-membered ring containing one nitrogen atom. The presence of a 4-fluorophenoxy group attached to the piperidine at the 3-position contributes to its unique properties. This compound is typically a white to off-white solid and is soluble in organic solvents, reflecting its moderate polarity. The fluorine atom in the phenoxy group can influence the compound's electronic properties, potentially enhancing its biological activity or altering its interaction with biological targets. 3-[(4-Fluorophenoxy)methyl]piperidine is of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential applications in treating various conditions. Its structure allows for the possibility of forming hydrogen bonds and engaging in π-π interactions, which are crucial for binding to biological receptors. As with many piperidine derivatives, it may exhibit a range of pharmacological activities, making it a subject of research in drug discovery and development.

CAS 142220-38-0

3-[(4-fluorophenoxy)methyl]piperidine

3-[(4-fluorophenoxy)methyl]piperidine

Ref: IN-DA001I0N

3-[(4-fluorophenoxy)methyl]piperidine

Ref: 10-F308536