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CAS 913835-52-6

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[4-(acetylsulfamoyl)phenyl]boronic acid

Description:
[4-(Acetylsulfamoyl)phenyl]boronic acid is an organic compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that also contains an acetylsulfamoyl substituent. This compound typically exhibits properties associated with both boronic acids and sulfonamides, including the ability to form reversible covalent bonds with diols, making it useful in various applications such as drug development and molecular recognition. The presence of the acetylsulfamoyl group enhances its solubility and reactivity, potentially allowing for interactions with biological targets. In terms of physical properties, it is likely to be a solid at room temperature, with moderate stability under standard conditions. The compound may also exhibit specific reactivity patterns in organic synthesis, particularly in cross-coupling reactions, due to the boron atom's ability to participate in nucleophilic attacks. Overall, [4-(acetylsulfamoyl)phenyl]boronic acid represents a versatile building block in medicinal chemistry and materials science.
Formula:C8H10BNO5S
InChI:InChI=1/C8H10BNO5S/c1-6(11)10-16(14,15)8-4-2-7(3-5-8)9(12)13/h2-5,12-13H,1H3,(H,10,11)
SMILES:CC(=NS(=O)(=O)c1ccc(cc1)B(O)O)O
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