Boronic acid, specifically 4-[(1,1-dimethylethyl)thio]phenyl- (CAS 820972-68-7), 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 thioether group. This compound typically exhibits a white to off-white solid appearance and is soluble in polar organic solvents. The presence of the boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis and materials science. The thioether substituent enhances the compound's stability and may influence its reactivity and solubility. Boronic acids are known for their ability to form reversible complexes with diols, making them useful in sensor applications and drug design. Additionally, this compound may exhibit unique biological properties, making it of interest in medicinal chemistry. Overall, its structural features contribute to its utility in synthetic organic chemistry and potential applications in pharmaceuticals.

Boronic acid, [4-[(1,1-dimethylethyl)thio]phenyl]-

820972-68-7: 4-(Tert-Butylthio) Phenylboronic Acid

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CAS 820972-68-7: Boronic acid, [4-[(1,1-dimethylethyl)thio]phenyl]-

4-(tert-Butylthio)phenylboronic acid

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4-(tert-Butylthio)phenylboronic Acid

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4-(tert-Butylthio)phenylboronic acid

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(4-(tert-Butylthio)phenyl)boronic acid

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4-(tert-Butylthio)phenylboronic acid

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