4-Phenyl-1-piperazineethanol is an organic compound characterized by its piperazine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms. This compound features a phenyl group attached to the piperazine, contributing to its aromatic properties, and an ethanol moiety that introduces hydroxyl functionality. The presence of the hydroxyl group enhances its solubility in polar solvents and can influence its reactivity and interaction with biological systems. Typically, compounds like 4-Phenyl-1-piperazineethanol may exhibit pharmacological activity, often being investigated for their potential use in medicinal chemistry, particularly in the development of psychoactive drugs or as intermediates in the synthesis of more complex molecules. Its molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can affect its biological activity and binding affinity to receptors. As with many piperazine derivatives, it may also display properties relevant to central nervous system activity, making it of interest in neuropharmacology. Safety and handling precautions should be observed, as with all chemical substances.

4-Phenyl-1-piperazineethanol

36245-26-8: 4-Phenyl-1-piperazineethanol is an organic compound characterized by its piperazine ring, which is a six-membered heterocyclic structure containing two nitrogen atoms. This compound features a phenyl group attached to the piperazine, contributing to its aromatic properties, and an ethanol moiety that introduces hydroxyl functionality. The presence of the hydroxyl group enhances its solubility in polar solvents and can influence its reactivity and interaction with biological systems. Typically, compounds like 4-Phenyl-1-piperazineethanol may exhibit pharmacological activity, often being investigated for their potential use in medicinal chemistry, particularly in the development of psychoactive drugs or as intermediates in the synthesis of more complex molecules. Its molecular structure allows for various interactions, including hydrogen bonding and π-π stacking, which can affect its biological activity and binding affinity to receptors. As with many piperazine derivatives, it may also display properties relevant to central nervous system activity, making it of interest in neuropharmacology. Safety and handling precautions should be observed, as with all chemical substances.

CAS 36245-26-8

4-Phenyl-1-piperazineethanol

2-(4-Phenylpiperazin-1-yl)ethan-1-ol

Ref: 3D-LBA24526