CAS 850568-77-3
:[4-(2-hydroxyethylsulfamoyl)phenyl]boronic acid
Description:
[4-(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 hydroxyethylsulfamoyl moiety, which enhances its solubility and reactivity. The presence of 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 pH and the presence of other functional groups, making it a versatile building block in chemical synthesis and research.
Formula:C8H12BNO5S
InChI:InChI=1/C8H12BNO5S/c11-6-5-10-16(14,15)8-3-1-7(2-4-8)9(12)13/h1-4,10-13H,5-6H2
SMILES:c1cc(ccc1B(O)O)S(=O)(=O)NCCO
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Found 3 products.
(4-(n-(2-Hydroxyethyl)sulfamoyl)phenyl)boronic acid
CAS:Formula:C8H12BNO5SPurity:98%Color and Shape:SolidMolecular weight:245.06064-[N-(2-Hydroxyethyl)sulphamoyl]benzeneboronic acid
CAS:<p>4-[N-(2-Hydroxyethyl)sulphamoyl]benzeneboronic acid</p>Formula:C8H12BNO5SPurity:95%Color and Shape: white solidMolecular weight:245.06g/mol


