B-(4-Cyano-3-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that contains both a cyano and a methoxy substituent. This compound typically exhibits properties such as being a white to off-white solid at room temperature, with solubility in polar organic solvents like methanol and dimethyl sulfoxide. The cyano group contributes to its electronic properties, potentially enhancing its reactivity in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and materials science. The methoxy group can influence the compound's polarity and reactivity, making it useful in medicinal chemistry and the development of pharmaceuticals. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug delivery systems. Overall, B-(4-Cyano-3-methoxyphenyl)boronic acid is a versatile compound with applications in organic synthesis, materials science, and medicinal chemistry.

B-(4-Cyano-3-methoxyphenyl)boronic acid

677777-45-6: 4-Cyano-3-methoxyphenylboronic acid, B-(4-Cyano-3-methoxyphenyl)boronic acid, Boronic acid, (4-cyano-3-methoxyphenyl)-, Boronic acid, B-(4-cyano-3-methoxyphenyl)-

(4-Cyano-3-methoxyphenyl)boronic acid

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CAS 677777-45-6: B-(4-Cyano-3-methoxyphenyl)boronic acid

(4-Cyano-3-methoxyphenyl)boronic acid

Ref: 10-F219655

4-Cyano-3-methoxyphenylboronic acid

Ref: 3D-FC160629

4-Cyano-3-methoxyphenylboronic acid

Ref: 54-OR360261

Boronic acid, (4-cyano-3-methoxyphenyl)- (9CI)

Ref: IN-DA006J8A