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CAS 913835-57-1

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[3-(2-hydroxyethylsulfamoyl)phenyl]boronic acid

Description:
[3-(2-hydroxyethylsulfamoyl)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 sulfonamide group, specifically a 2-hydroxyethylsulfamoyl moiety, which enhances its solubility and reactivity. The hydroxyl group contributes to its potential as a ligand in various chemical reactions, particularly in the context of medicinal chemistry and drug development. Boronic acids are often utilized in Suzuki coupling reactions, making this compound valuable in synthetic organic chemistry. Additionally, the sulfonamide group may impart biological activity, suggesting potential applications in pharmaceuticals. The compound's properties, such as solubility, stability, and reactivity, can be influenced by the pH of the environment, as boronic acids can exist in different forms depending on the protonation state. Overall, [3-(2-hydroxyethylsulfamoyl)phenyl]boronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C8H12BNO5S
InChI:InChI=1/C8H12BNO5S/c11-5-4-10-16(14,15)8-3-1-2-7(6-8)9(12)13/h1-3,6,10-13H,4-5H2
SMILES:c1cc(cc(c1)S(=O)(=O)NCCO)B(O)O
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