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CAS 871329-58-7

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[3-(diethylsulfamoyl)phenyl]boronic acid

Description:
[3-(Diethylsulfamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a diethylsulfamoyl group. 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 organic synthesis and medicinal chemistry. The diethylsulfamoyl moiety contributes to its solubility and reactivity, enhancing its potential as a ligand in coordination chemistry. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The compound's structure suggests it may have biological activity, potentially serving as a pharmacophore in drug development. Its stability, reactivity, and solubility in polar solvents are important characteristics that influence its applications in research and industry. As with many boronic acids, care must be taken in handling due to their sensitivity to moisture and air.
Formula:C10H16BNO4S
InChI:InChI=1/C10H16BNO4S/c1-3-12(4-2)17(15,16)10-7-5-6-9(8-10)11(13)14/h5-8,13-14H,3-4H2,1-2H3
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