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CAS 1402238-36-1

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B-[4-(Aminosulfonyl)-2-methylphenyl]boronic acid

Description:
B-[4-(Aminosulfonyl)-2-methylphenyl]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 sulfonamide group, which contributes to its potential biological activity, particularly in medicinal chemistry. The presence of the methyl group on the aromatic ring influences its solubility and reactivity. Boronic acids are often utilized in various applications, including organic synthesis, drug development, and as tools in biochemical research due to their ability to interact with biomolecules. The specific structure of this compound suggests potential applications in targeting specific enzymes or receptors, particularly in the context of cancer research or other therapeutic areas. Additionally, the compound's properties, such as solubility, stability, and reactivity, can be influenced by pH and the presence of other functional groups, making it a versatile candidate for further study in both synthetic and medicinal chemistry.
Formula:C7H10BNO4S
InChI:InChI=1S/C7H10BNO4S/c1-5-4-6(14(9,12)13)2-3-7(5)8(10)11/h2-4,10-11H,1H3,(H2,9,12,13)
InChI key:InChIKey=BSLOFCDDCNUTDZ-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=CC(C)=C(B(O)O)C=C1
Synonyms:
  • B-[4-(Aminosulfonyl)-2-methylphenyl]boronic acid
  • Boronic acid, B-[4-(aminosulfonyl)-2-methylphenyl]-
  • (2-Methyl-4-sulfamoylphenyl)boronic acid
  • 2-Methyl-4-sulfamoylbenzeneboronic acid
  • 2-Methyl-4-sulphamoylbenzeneboronicacid
  • 2-Methyl-4-sulfamoylphenylboronic acid
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