Boronic acid, specifically 4-formyl-3-methylphenyl boronic acid, is an organic compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that also contains a formyl group (-CHO) and a methyl group (-CH3). This compound typically exhibits properties associated with 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 presence of the formyl group introduces reactivity that can facilitate further chemical transformations, while the methyl group can influence the compound's solubility and steric properties. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, this compound may exhibit moderate acidity due to the boronic acid moiety, allowing it to participate in acid-base reactions. Overall, the unique combination of functional groups in this compound provides a versatile platform for further chemical exploration and application in synthetic methodologies.

Boronic acid,(4-formyl-3-methylphenyl)- (9CI)

398151-59-2: Boronic acid, specifically 4-formyl-3-methylphenyl boronic acid, is an organic compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that also contains a formyl group (-CHO) and a methyl group (-CH3). This compound typically exhibits properties associated with 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 presence of the formyl group introduces reactivity that can facilitate further chemical transformations, while the methyl group can influence the compound's solubility and steric properties. Boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, this compound may exhibit moderate acidity due to the boronic acid moiety, allowing it to participate in acid-base reactions. Overall, the unique combination of functional groups in this compound provides a versatile platform for further chemical exploration and application in synthetic methodologies.

CAS 398151-59-2

Boronic acid,(4-formyl-3-methylphenyl)- (9CI)

4-Formyl-3-methylphenylboronic acid

Ref: IN-DA00777G

4-Formyl-3-methylphenylboronic acid

Ref: 54-OR360248

(4-Formyl-3-methylphenyl)boronic acid

Ref: 10-F338080