Description:3-Cyanophenylboronic acid is an organoboron compound characterized by the presence of both a boronic acid functional group and a cyano group attached to a phenyl ring. Its molecular structure features a boron atom bonded to a hydroxyl group and a phenyl ring that is further substituted with a cyano group at the meta position. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The cyano group contributes to its electronic properties, enhancing its reactivity in certain chemical transformations. 3-Cyanophenylboronic acid is often utilized in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it may have potential applications in materials science and as a building block in the development of pharmaceuticals.
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