1-(4-Benzyloxy-3-methoxy-phenyl)-piperazine is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. This compound features a phenyl group substituted with both a benzyloxy and a methoxy group, contributing to its lipophilicity and potential biological activity. The presence of the benzyloxy group enhances its solubility in organic solvents, while the methoxy group can influence its electronic properties and reactivity. The compound is often studied for its pharmacological properties, particularly in relation to its interactions with neurotransmitter systems, which may suggest potential applications in medicinal chemistry. Its molecular structure allows for various conformations, which can affect its binding affinity to biological targets. Additionally, the compound's synthesis typically involves multi-step organic reactions, highlighting its complexity. As with many piperazine derivatives, it may exhibit a range of biological activities, making it of interest in drug development and research. Safety and handling precautions should be observed due to its chemical nature.

1-(4-BENZYLOXY-3-METHOXY-PHENYL)-PIPERAZINE

142353-49-9: 1-(4-Benzyloxy-3-methoxy-phenyl)-piperazine is a chemical compound characterized by its piperazine core, which is a six-membered ring containing two nitrogen atoms. This compound features a phenyl group substituted with both a benzyloxy and a methoxy group, contributing to its lipophilicity and potential biological activity. The presence of the benzyloxy group enhances its solubility in organic solvents, while the methoxy group can influence its electronic properties and reactivity. The compound is often studied for its pharmacological properties, particularly in relation to its interactions with neurotransmitter systems, which may suggest potential applications in medicinal chemistry. Its molecular structure allows for various conformations, which can affect its binding affinity to biological targets. Additionally, the compound's synthesis typically involves multi-step organic reactions, highlighting its complexity. As with many piperazine derivatives, it may exhibit a range of biological activities, making it of interest in drug development and research. Safety and handling precautions should be observed due to its chemical nature.

CAS 142353-49-9

1-(4-BENZYLOXY-3-METHOXY-PHENYL)-PIPERAZINE

1-(4-BENZYLOXY-3-METHOXY-PHENYL)-PIPERAZINE

Ref: IN-DA007YTS

1-(4-Benzyloxy-3-methoxy-phenyl)-piperazine

Ref: 10-F036921