4-Piperidin-1-ylbenzoate, with the CAS number 22090-24-0, is an organic compound characterized by its piperidine ring and benzoate moiety. It features a piperidine group, which is a six-membered saturated nitrogen-containing heterocycle, attached to a benzoate structure, indicating that it is an ester derived from benzoic acid. This compound typically exhibits properties such as moderate solubility in organic solvents and potential bioactivity due to the presence of the piperidine ring, which is often associated with various pharmacological effects. The molecular structure suggests that it may participate in hydrogen bonding and other intermolecular interactions, influencing its reactivity and stability. Additionally, compounds like 4-piperidin-1-ylbenzoate may be of interest in medicinal chemistry for their potential applications in drug development, particularly in the synthesis of pharmaceuticals targeting the central nervous system or other biological pathways. As with many organic compounds, its physical and chemical properties, such as melting point, boiling point, and reactivity, would depend on the specific conditions and environment in which it is studied.

4-piperidin-1-ylbenzoate

22090-24-0: 4-Piperidin-1-ylbenzoate, with the CAS number 22090-24-0, is an organic compound characterized by its piperidine ring and benzoate moiety. It features a piperidine group, which is a six-membered saturated nitrogen-containing heterocycle, attached to a benzoate structure, indicating that it is an ester derived from benzoic acid. This compound typically exhibits properties such as moderate solubility in organic solvents and potential bioactivity due to the presence of the piperidine ring, which is often associated with various pharmacological effects. The molecular structure suggests that it may participate in hydrogen bonding and other intermolecular interactions, influencing its reactivity and stability. Additionally, compounds like 4-piperidin-1-ylbenzoate may be of interest in medicinal chemistry for their potential applications in drug development, particularly in the synthesis of pharmaceuticals targeting the central nervous system or other biological pathways. As with many organic compounds, its physical and chemical properties, such as melting point, boiling point, and reactivity, would depend on the specific conditions and environment in which it is studied.

CAS 22090-24-0

4-piperidin-1-ylbenzoate

4-(Piperidin-1-yl)benzoic acid

Ref: IN-DA007PMU

4-(Piperidin-1-yl)benzoic acid

Ref: 54-OR0759

4-Piperidin-1-yl-benzoic acid

Ref: 10-F055289