4-(Pyridin-3-yl)phenylboronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and a pyridine ring. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. It has applications in organic synthesis, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. The presence of the pyridine moiety can enhance its reactivity and selectivity in various chemical transformations. Additionally, the compound may exhibit properties such as moderate acidity due to the boronic acid group, allowing it to participate in acid-base reactions. Its structural features also suggest potential interactions with biological systems, making it of interest in medicinal chemistry. Overall, 4-(Pyridin-3-yl)phenylboronic acid is a versatile compound with significant utility in both synthetic and biological chemistry.

4-(Pyridin-3-yl)phenylboronic acid

170230-28-1: 4-(3-Pyridinyl)phenylboronic acid, B-[4-(3-Pyridinyl)phenyl]boronic acid, Boronic acid, B-[4-(3-pyridinyl)phenyl]-, Boronic acid, [4-(3-pyridinyl)phenyl]-, [4-(3-Pyridyl)phenyl]boronic acid, 4-(Pyridin-3-yl)phenylboronic acid

(4-(Pyridin-3-yl)phenyl)boronic acid

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CAS 170230-28-1: 4-(Pyridin-3-yl)phenylboronic acid

(4-(Pyridin-3-yl)phenyl)boronic acid

Ref: 10-F327538

4-(Pyridin-3-yl)phenylboronic acid

Ref: 3D-FP158548

4-(Pyridin-3-yl)Phenylboronic Acid

Ref: 54-OR1011196

4-(pyridin-3-yl)phenylboronic acid

Ref: IN-DA00APVQ