1-(2-Fluoroethyl)piperidin-4-ol is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a hydroxyl group (-OH) at the 4-position of the piperidine ring contributes to its potential as a secondary amine, influencing its reactivity and solubility in polar solvents. The 2-fluoroethyl substituent introduces a fluorine atom, which can enhance the compound's lipophilicity and may affect its biological activity. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as the fluorine atom can modulate pharmacokinetic properties. Additionally, the presence of both the hydroxyl and fluorinated groups may impart unique interactions with biological targets, making it a candidate for further research in therapeutic contexts. Its molecular structure and functional groups suggest that it may participate in hydrogen bonding and other intermolecular interactions, which are critical for its behavior in biological systems.

1-(2-fluoroethyl)piperidin-4-ol

492446-45-4: 1-(2-Fluoroethyl)piperidin-4-ol is a chemical compound characterized by its piperidine ring structure, which is a six-membered saturated nitrogen-containing heterocycle. The presence of a hydroxyl group (-OH) at the 4-position of the piperidine ring contributes to its potential as a secondary amine, influencing its reactivity and solubility in polar solvents. The 2-fluoroethyl substituent introduces a fluorine atom, which can enhance the compound's lipophilicity and may affect its biological activity. This compound is of interest in medicinal chemistry, particularly for its potential applications in drug development, as the fluorine atom can modulate pharmacokinetic properties. Additionally, the presence of both the hydroxyl and fluorinated groups may impart unique interactions with biological targets, making it a candidate for further research in therapeutic contexts. Its molecular structure and functional groups suggest that it may participate in hydrogen bonding and other intermolecular interactions, which are critical for its behavior in biological systems.

CAS 492446-45-4

1-(2-fluoroethyl)piperidin-4-ol

1-(2-Fluoroethyl)piperidin-4-ol

Ref: IN-DA00DHX9

1-(2-Fluoroethyl)-4-hydroxypiperidine

Ref: 54-PC3464