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CAS 871329-65-6

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[4-(ethylsulfamoyl)phenyl]boronic acid

Description:
[4-(ethylsulfamoyl)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 an ethylsulfamoyl 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 medicinal chemistry and materials science. The ethylsulfamoyl group enhances its solubility and may contribute to its biological activity. In terms of physical properties, it is likely to be a solid at room temperature, with moderate solubility in polar solvents due to the presence of both hydrophobic and hydrophilic regions. The compound may also exhibit acidic behavior, as boronic acids can donate protons under certain conditions. Its unique structure allows it to participate in Suzuki-Miyaura cross-coupling reactions, which are valuable in the synthesis of complex organic molecules. Overall, [4-(ethylsulfamoyl)phenyl]boronic acid is a versatile compound with potential applications in drug development and organic synthesis.
Formula:C8H12BNO4S
InChI:InChI=1/C8H12BNO4S/c1-2-10-15(13,14)8-5-3-7(4-6-8)9(11)12/h3-6,10-12H,2H2,1H3
SMILES:CCNS(=O)(=O)c1ccc(cc1)B(O)O
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