[4-(Dimethylsulfamoyl)-2-methyl-phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols. This compound features a phenyl ring substituted with a dimethylsulfamoyl group and a methyl group, contributing to its unique chemical properties. The dimethylsulfamoyl moiety enhances its solubility and reactivity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The boronic acid group also plays a significant role in medicinal chemistry, as it can interact with biological molecules, potentially influencing enzyme activity or serving as a pharmacophore in drug design. Additionally, the compound's structure suggests it may exhibit specific steric and electronic properties, which can affect its reactivity and interactions in different chemical environments. Overall, this compound is of interest in both synthetic organic chemistry and pharmaceutical applications.

[4-(dimethylsulfamoyl)-2-methyl-phenyl]boronic acid

957034-82-1: (4-(N,N-Dimethylsulfamoyl)-2-methylphenyl)boronicacid

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CAS 957034-82-1: [4-(dimethylsulfamoyl)-2-methyl-phenyl]boronic acid

4-(N,N-Dimethylsulfamoyl)-2-methylphenylboronic acid

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(4-(N,N-Dimethylsulfamoyl)-2-methylphenyl)boronic acid

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