Boronic acid, specifically 3-(phenylmethyl)phenylboronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a phenylmethyl group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under ambient conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. Its structure contributes to its reactivity, enabling it to form complexes with diols and other Lewis bases. Additionally, boronic acids are known for their ability to act as pH-sensitive compounds, which can be useful in drug delivery systems and sensor applications. Overall, this compound's unique characteristics stem from its boron content and the presence of aromatic rings, which influence its chemical behavior and potential applications in various fields.

Boronic acid, [3-(phenylmethyl)phenyl]-(9CI)

173394-24-6: Boronic acid, specifically 3-(phenylmethyl)phenylboronic acid, is an organoboron compound characterized by the presence of a boronic acid functional group (-B(OH)2) attached to a phenyl ring that is further substituted with a phenylmethyl group. This compound typically exhibits properties such as being a white to off-white solid, soluble in polar organic solvents, and possessing moderate stability under ambient conditions. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. Its structure contributes to its reactivity, enabling it to form complexes with diols and other Lewis bases. Additionally, boronic acids are known for their ability to act as pH-sensitive compounds, which can be useful in drug delivery systems and sensor applications. Overall, this compound's unique characteristics stem from its boron content and the presence of aromatic rings, which influence its chemical behavior and potential applications in various fields.

CAS 173394-24-6

Boronic acid, [3-(phenylmethyl)phenyl]-(9CI)

Boronic acid, [3-(phenylmethyl)phenyl]- (9CI)

Ref: IN-DA001YUD

(3-Benzylphenyl)boronic acid

Ref: 54-OR1057486

(3-Benzylphenyl)boronic acid

Ref: 10-F634252