Boronic acid, specifically 3-fluoro-4-(methylsulfonyl)phenyl boronic 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 substituted with a fluoro group and a methylsulfonyl group. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid functionality. The presence of the fluoro group can influence its electronic properties and reactivity, while the methylsulfonyl group may enhance its solubility and stability. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis, medicinal chemistry, and as intermediates in the preparation of pharmaceuticals. Additionally, the specific structural features of this compound may contribute to its potential biological activity and utility in drug development.

Boronic acid, [3-fluoro-4-(methylsulfonyl)phenyl]-

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3-FLUORO-4-(METHYLSULFONYL)PHENYLBORONIC ACID

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[3-Fluoro-4-(methylsulfonyl)phenyl]boronic acid

(3-Fluoro-4-(methylsulfonyl)phenyl)boronic acid

3-Fluoro-4-(methylsulphonyl)benzeneboronic acid

CAS 648904-83-0: Boronic acid, [3-fluoro-4-(methylsulfonyl)phenyl]-

3-FLUORO-4-(METHYLSULFONYL)PHENYLBORONIC ACID

Ref: IN-DA003JFG

[3-Fluoro-4-(methylsulfonyl)phenyl]boronic acid

Ref: 3D-FF90639

(3-Fluoro-4-(methylsulfonyl)phenyl)boronic acid

Ref: 10-F211028

3-Fluoro-4-(methylsulphonyl)benzeneboronic acid

Ref: 54-PC3656