1-[3-Fluoro-4-(3-methylpiperidin-1-yl)phenyl]ethanamine, with the CAS number 1332529-03-9, is a chemical compound characterized by its unique structure that includes a phenyl ring substituted with a fluorine atom and a piperidine moiety. This compound features an ethanamine functional group, which contributes to its potential as a biological agent. The presence of the fluorine atom may enhance lipophilicity and influence the compound's interaction with biological targets, potentially affecting its pharmacological properties. The 3-methylpiperidine component adds to the steric and electronic characteristics of the molecule, which can impact its binding affinity and selectivity for specific receptors or enzymes. Such compounds are often studied for their potential therapeutic applications, particularly in the fields of neuroscience and medicinal chemistry, where modifications to amine structures can lead to varied biological activities. Overall, the unique combination of functional groups in this compound suggests a complex profile that warrants further investigation in drug development and related research.

1-[3-fluoro-4-(3-methylpiperidin-1-yl)phenyl]ethanamine

1332529-03-9: 1-[3-Fluoro-4-(3-methylpiperidin-1-yl)phenyl]ethanamine, with the CAS number 1332529-03-9, is a chemical compound characterized by its unique structure that includes a phenyl ring substituted with a fluorine atom and a piperidine moiety. This compound features an ethanamine functional group, which contributes to its potential as a biological agent. The presence of the fluorine atom may enhance lipophilicity and influence the compound's interaction with biological targets, potentially affecting its pharmacological properties. The 3-methylpiperidine component adds to the steric and electronic characteristics of the molecule, which can impact its binding affinity and selectivity for specific receptors or enzymes. Such compounds are often studied for their potential therapeutic applications, particularly in the fields of neuroscience and medicinal chemistry, where modifications to amine structures can lead to varied biological activities. Overall, the unique combination of functional groups in this compound suggests a complex profile that warrants further investigation in drug development and related research.

CAS 1332529-03-9

1-[3-fluoro-4-(3-methylpiperidin-1-yl)phenyl]ethanamine