[3-(Dimethylsulfamoylamino)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains a dimethylsulfamoyl amino substituent. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including medicinal chemistry and materials science. The dimethylsulfamoyl group enhances its solubility and reactivity, potentially influencing its biological activity. The compound may also participate in Suzuki coupling reactions, which are valuable in the synthesis of complex organic molecules. Its structure suggests potential applications in drug development, particularly in targeting specific biological pathways. Additionally, the presence of the boron atom can impart unique electronic properties, making it a subject of interest in the study of organoboron chemistry. Overall, [3-(dimethylsulfamoylamino)phenyl]boronic acid is a versatile compound with significant implications in both research and practical applications.

[3-(dimethylsulfamoylamino)phenyl]boronic acid

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CAS 277295-50-8: [3-(dimethylsulfamoylamino)phenyl]boronic acid

(3-((N,N-Dimethylsulfamoyl)-amino)phenyl)boronic acid

Ref: 3D-FN160508

3-(N,N-Dimethylsulphamoylamino)benzeneboronic acid

Ref: 54-OR9571

Boronic acid, B-[3-[[(dimethylamino)sulfonyl]amino]phenyl]-

Ref: IN-DA002ULS