2-(3-Fluorophenyl)piperidine is an organic compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a 3-fluorophenyl group indicates that a fluorine atom is substituted on the phenyl ring at the meta position relative to the piperidine attachment. This compound typically exhibits properties such as moderate solubility in organic solvents and potential biological activity, making it of interest in medicinal chemistry. Its structure suggests that it may interact with various biological targets, potentially influencing neurotransmitter systems. The fluorine atom can enhance lipophilicity and metabolic stability, which are important factors in drug design. Additionally, 2-(3-fluorophenyl)piperidine may undergo typical reactions associated with piperidine derivatives, including alkylation and acylation, allowing for further functionalization. Safety and handling considerations should be observed, as with many organic compounds, due to potential toxicity and reactivity. Overall, this compound represents a valuable scaffold for the development of pharmaceuticals and research into its chemical behavior and biological effects.

2-(3-fluorophenyl)piperidine

383128-42-5: 2-(3-Fluorophenyl)piperidine is an organic compound characterized by its piperidine ring, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a 3-fluorophenyl group indicates that a fluorine atom is substituted on the phenyl ring at the meta position relative to the piperidine attachment. This compound typically exhibits properties such as moderate solubility in organic solvents and potential biological activity, making it of interest in medicinal chemistry. Its structure suggests that it may interact with various biological targets, potentially influencing neurotransmitter systems. The fluorine atom can enhance lipophilicity and metabolic stability, which are important factors in drug design. Additionally, 2-(3-fluorophenyl)piperidine may undergo typical reactions associated with piperidine derivatives, including alkylation and acylation, allowing for further functionalization. Safety and handling considerations should be observed, as with many organic compounds, due to potential toxicity and reactivity. Overall, this compound represents a valuable scaffold for the development of pharmaceuticals and research into its chemical behavior and biological effects.

CAS 383128-42-5

2-(3-fluorophenyl)piperidine

2-(3-Fluorophenyl)piperidine

Ref: IN-DA00BYO3

2-(3-Fluorophenyl)piperidine

Ref: 54-PC901105

2-(3-fluorophenyl)piperidine

Ref: 10-F308157