(R)-Piperidin-3-ol is a chiral organic compound characterized by a six-membered saturated ring containing a nitrogen atom and a hydroxyl group (-OH) at the third position. Its molecular structure features a piperidine ring, which contributes to its basicity and potential for forming hydrogen bonds. The presence of the hydroxyl group enhances its solubility in polar solvents and influences its reactivity, making it a valuable intermediate in organic synthesis and pharmaceutical applications. As a chiral molecule, (R)-Piperidin-3-ol can exhibit different biological activities compared to its enantiomer, which is significant in drug development. The compound is typically handled with standard safety precautions, as it may pose risks such as irritation upon contact with skin or eyes. Its applications may include roles in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals, highlighting its importance in both industrial and research settings.

(R)-Piperidin-3-ol

(R)-3-Piperidinol is a chiral molecule that exhibits optical activity. It is a synthetic compound that can be used as an actuator for ion channels and other biomolecules. The asymmetry of the molecule, which makes it optically active, is due to its homochiral nature. This property has been shown to be switchable, meaning that the optical activity can be switched on or off by using light or temperature changes. (R)-3-Piperidinol has been found to have biological properties such as acetylcholine release from neurons in the mouse brain and a switchable effect on potassium channels in rat neurons.

CAS 62414-68-0: (R)-Piperidin-3-ol

(R)-Piperidin-3-ol

Ref: 54-OR92074

(R)-3-Piperidinol

Ref: 3D-FP158464

(R)-Piperidin-3-ol

Ref: 10-F609500

(R)-Piperidin-3-ol

Ref: IN-DA00EIEG