3-(Piperidinyl)phenylboronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring, which is further substituted with a piperidine moiety. This compound typically exhibits properties associated with both boronic acids and amines, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as drug development and materials science. The piperidine ring contributes to its basicity and potential for forming hydrogen bonds, enhancing its solubility in polar solvents. Additionally, the compound may exhibit biological activity, particularly in the context of medicinal chemistry, where boronic acids are often explored for their role in enzyme inhibition and as building blocks in the synthesis of pharmaceuticals. Its structural features suggest potential interactions with biological targets, making it a candidate for further investigation in therapeutic contexts. Overall, 3-(Piperidinyl)phenylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.

3-(Piperidinyl)phenylboronic acid

634905-21-8: Boronic Acid, B-[3-(1-Piperidinyl)Phenyl]-, [3-(1-Piperidyl)Phenyl]Boronic Acid

CAS 634905-21-8: 3-(Piperidinyl)phenylboronic acid

3-(Piperidino)phenylboronic acid

Ref: 54-OR361547

BORONIC ACID, B-[3-(1-PIPERIDINYL)PHENYL]-

Ref: IN-DA00EBNS

3-(Piperidino)phenylboronic acid

Ref: 3D-JAB90521

(3-(Piperidin-1-yl)phenyl)boronic acid

Ref: 10-F232277