Boronic acid, specifically B-(3-methoxy-5-methylphenyl)-, is an organoboron compound characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a methoxy and a methyl group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, which makes it useful in various applications, including organic synthesis and medicinal chemistry. The methoxy and methyl substituents enhance its solubility and reactivity, allowing for participation in cross-coupling reactions, such as Suzuki reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, boronic acids can act as Lewis acids, facilitating various catalytic processes. The compound's structure contributes to its potential biological activity, making it a subject of interest in drug development and material science. Overall, B-(3-methoxy-5-methylphenyl)boronic acid is a versatile building block in synthetic chemistry, with applications spanning pharmaceuticals and advanced materials.

Boronic acid,B-(3-methoxy-5-methylphenyl)-

725251-81-0: Boronicacid, (3-methoxy-5-methylphenyl)- (9CI), 3-Methoxy-5-methylphenylboronic acid, 5-Methyl-3-methoxyphenylboronic acid

(3-Methoxy-5-methylphenyl)boronic acid

3-Methoxy-5-methylphenylboronic acid

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CAS 725251-81-0: Boronic acid,B-(3-methoxy-5-methylphenyl)-

(3-Methoxy-5-methylphenyl)boronic acid

Ref: 10-F219657

3-Methoxy-5-methylphenylboronic acid

Ref: 54-OR360264

3-Methoxy-5-methylphenylboronic acid

Ref: 3D-FM160650

Boronic acid, (3-methoxy-5-methylphenyl)- (9CI)

Ref: IN-DA003BSP