Piperidine, 2-[[[3,4-dichlorophenyl)methoxy]methyl]-, hydrochloride (1:1) is a chemical compound characterized by its piperidine core, which is a six-membered saturated heterocyclic ring containing one nitrogen atom. The presence of the 3,4-dichlorophenyl group indicates that the compound has significant aromatic characteristics, contributing to its potential biological activity. The methoxy group attached to the phenyl ring enhances the compound's lipophilicity, which may influence its pharmacokinetic properties. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, facilitating its use in various applications, particularly in pharmaceuticals. The compound may exhibit various biological activities, making it of interest in medicinal chemistry. However, specific safety and handling guidelines should be followed due to the presence of chlorine substituents, which can impart toxicity. Overall, this compound's unique structure suggests potential utility in drug development, although further studies would be necessary to fully elucidate its properties and applications.

Piperidine, 2-[[(3,4-dichlorophenyl)methoxy]methyl]-, hydrochloride (1:1)

1289385-61-0: Piperidine, 2-[[[3,4-dichlorophenyl)methoxy]methyl]-, hydrochloride (1:1) is a chemical compound characterized by its piperidine core, which is a six-membered saturated heterocyclic ring containing one nitrogen atom. The presence of the 3,4-dichlorophenyl group indicates that the compound has significant aromatic characteristics, contributing to its potential biological activity. The methoxy group attached to the phenyl ring enhances the compound's lipophilicity, which may influence its pharmacokinetic properties. As a hydrochloride salt, it is typically more soluble in water compared to its free base form, facilitating its use in various applications, particularly in pharmaceuticals. The compound may exhibit various biological activities, making it of interest in medicinal chemistry. However, specific safety and handling guidelines should be followed due to the presence of chlorine substituents, which can impart toxicity. Overall, this compound's unique structure suggests potential utility in drug development, although further studies would be necessary to fully elucidate its properties and applications.

CAS 1289385-61-0

Piperidine, 2-[[(3,4-dichlorophenyl)methoxy]methyl]-, hydrochloride (1:1)