Boronic acid, specifically 2-(hydroxymethyl)-4-methoxyphenyl 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 hydroxymethyl and a methoxy substituent. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols due to the presence of hydroxyl groups. Its boronic acid functionality allows it to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a building block in the development of pharmaceuticals. The methoxy group enhances its lipophilicity, potentially influencing its biological activity and interaction with other molecules. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. Overall, this compound's unique structural features contribute to its versatility in chemical reactions and applications in material science and drug development.

Boronic acid,[2-(hydroxymethyl)-4-methoxyphenyl]- (9CI)

762263-92-3: Boronic acid, specifically 2-(hydroxymethyl)-4-methoxyphenyl 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 hydroxymethyl and a methoxy substituent. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar solvents like water and alcohols due to the presence of hydroxyl groups. Its boronic acid functionality allows it to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis, medicinal chemistry, and as a building block in the development of pharmaceuticals. The methoxy group enhances its lipophilicity, potentially influencing its biological activity and interaction with other molecules. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in forming carbon-carbon bonds in organic synthesis. Overall, this compound's unique structural features contribute to its versatility in chemical reactions and applications in material science and drug development.

CAS 762263-92-3

Boronic acid,[2-(hydroxymethyl)-4-methoxyphenyl]- (9CI)

2-Hydroxymethyl-4-methoxyphenylboronic acid

Ref: IN-DA005RJE

2-Hydroxymethyl-4-methoxyphenylboronic acid

Ref: 54-OR360267

(2-(Hydroxymethyl)-4-methoxyphenyl)boronic acid

Ref: 10-F219660