4-Piperidyl(2-thienyl)methanol is a chemical compound characterized by its unique structure, which includes a piperidine ring and a thienyl group. The piperidine moiety contributes to its potential as a pharmacophore, often associated with various biological activities, including analgesic and anti-inflammatory effects. The thienyl group, derived from thiophene, adds to the compound's aromatic character and may influence its electronic properties and interactions with biological targets. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the hydroxyl (-OH) group. Its molecular structure suggests potential for hydrogen bonding, which can affect its reactivity and interactions in biological systems. Additionally, the presence of both a nitrogen atom in the piperidine ring and the hydroxyl group may enhance its ability to form complexes with various biomolecules. Overall, 4-piperidyl(2-thienyl)methanol is of interest in medicinal chemistry for its potential therapeutic applications, although specific biological activities and mechanisms would require further investigation.

4-piperidyl(2-thienyl)methanol

938458-94-7: 4-Piperidyl(2-thienyl)methanol is a chemical compound characterized by its unique structure, which includes a piperidine ring and a thienyl group. The piperidine moiety contributes to its potential as a pharmacophore, often associated with various biological activities, including analgesic and anti-inflammatory effects. The thienyl group, derived from thiophene, adds to the compound's aromatic character and may influence its electronic properties and interactions with biological targets. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the hydroxyl (-OH) group. Its molecular structure suggests potential for hydrogen bonding, which can affect its reactivity and interactions in biological systems. Additionally, the presence of both a nitrogen atom in the piperidine ring and the hydroxyl group may enhance its ability to form complexes with various biomolecules. Overall, 4-piperidyl(2-thienyl)methanol is of interest in medicinal chemistry for its potential therapeutic applications, although specific biological activities and mechanisms would require further investigation.

CAS 938458-94-7

4-piperidyl(2-thienyl)methanol

piperidin-4-yl(2-thienyl)methanol

Ref: 10-F308639