2-(4-Methylpiperazin-1-yl)cyclopentanamine is a chemical compound characterized by its unique structure, which includes a cyclopentane ring and a piperazine moiety. The presence of the piperazine ring, which is a six-membered nitrogen-containing heterocycle, contributes to its potential biological activity, often associated with pharmacological properties. The methyl group on the piperazine enhances its lipophilicity, potentially influencing its ability to cross biological membranes. This compound may exhibit various functional properties, including being a potential ligand for receptors or enzymes, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests it may participate in hydrogen bonding due to the amine groups, which can affect its solubility and reactivity. Additionally, the compound's specific stereochemistry and functional groups can influence its interaction with biological targets, making it a candidate for further research in therapeutic applications. As with many amines, it may also exhibit basic properties, allowing it to form salts with acids.

2-(4-methylpiperazin-1-yl)cyclopentanamine

953895-57-3: 2-(4-Methylpiperazin-1-yl)cyclopentanamine is a chemical compound characterized by its unique structure, which includes a cyclopentane ring and a piperazine moiety. The presence of the piperazine ring, which is a six-membered nitrogen-containing heterocycle, contributes to its potential biological activity, often associated with pharmacological properties. The methyl group on the piperazine enhances its lipophilicity, potentially influencing its ability to cross biological membranes. This compound may exhibit various functional properties, including being a potential ligand for receptors or enzymes, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests it may participate in hydrogen bonding due to the amine groups, which can affect its solubility and reactivity. Additionally, the compound's specific stereochemistry and functional groups can influence its interaction with biological targets, making it a candidate for further research in therapeutic applications. As with many amines, it may also exhibit basic properties, allowing it to form salts with acids.

CAS 953895-57-3

2-(4-methylpiperazin-1-yl)cyclopentanamine