Boronic acid, specifically 4-[(trimethylsilyl)ethynyl]phenyl-, 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 trimethylsilyl group and an ethynyl group. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. The presence of the boronic acid moiety allows for participation in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The trimethylsilyl group enhances the stability and solubility of the compound, while the ethynyl group can serve as a reactive site for further functionalization. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in various applications, including sensor technology and drug delivery systems. Overall, this compound is significant in synthetic organic chemistry and materials science due to its versatile reactivity and functional properties.

Boronic acid, [4-[(trimethylsilyl)ethynyl]phenyl]-

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(4-[(Trimethylsilyl)ethynyl]phenyl)boronic acid

CAS 630127-51-4: Boronic acid, [4-[(trimethylsilyl)ethynyl]phenyl]-

(4-[(Trimethylsilyl)ethynyl]phenyl)boronic acid

Ref: 54-OR360469

(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid

Ref: 3D-FAB12751

(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid

Ref: IN-DA003BTW

(4-((Trimethylsilyl)ethynyl)phenyl)boronic acid

Ref: 10-F218633

(4-[(Trimethylsilyl)ethynyl]phenyl)boronic Acid

Ref: TR-T900203