3-Piperidin-1-ylbenzonitrile, identified by its CAS number 175696-74-9, is an organic compound characterized by the presence of a piperidine ring and a benzonitrile moiety. The piperidine ring is a six-membered saturated nitrogen-containing heterocycle, which contributes to the compound's basicity and potential for forming hydrogen bonds. The benzonitrile part of the molecule features a phenyl group attached to a cyano group, which imparts significant polarity and can influence the compound's reactivity and solubility. This compound is typically used in medicinal chemistry and drug development due to its potential biological activity, particularly in the context of targeting specific receptors or enzymes. Its structural features suggest it may exhibit properties such as lipophilicity, which can affect its pharmacokinetics and bioavailability. Additionally, the presence of both the piperidine and nitrile functionalities may allow for diverse chemical modifications, making it a versatile scaffold in synthetic organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

3-PIPERIDIN-1-YLBENZONITRILE

175696-74-9: 3-Piperidin-1-ylbenzonitrile, identified by its CAS number 175696-74-9, is an organic compound characterized by the presence of a piperidine ring and a benzonitrile moiety. The piperidine ring is a six-membered saturated nitrogen-containing heterocycle, which contributes to the compound's basicity and potential for forming hydrogen bonds. The benzonitrile part of the molecule features a phenyl group attached to a cyano group, which imparts significant polarity and can influence the compound's reactivity and solubility. This compound is typically used in medicinal chemistry and drug development due to its potential biological activity, particularly in the context of targeting specific receptors or enzymes. Its structural features suggest it may exhibit properties such as lipophilicity, which can affect its pharmacokinetics and bioavailability. Additionally, the presence of both the piperidine and nitrile functionalities may allow for diverse chemical modifications, making it a versatile scaffold in synthetic organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

CAS 175696-74-9

3-PIPERIDIN-1-YLBENZONITRILE

3-Piperidin-1-ylbenzonitrile

Ref: IN-DA00213P

3-Piperidin-1-ylbenzonitrile

Ref: 54-OR4433