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CAS 874219-48-4

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[4-(3-chloropropylsulfamoyl)phenyl]boronic acid

Description:
[4-(3-Chloropropylsulfamoyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a sulfamoyl group, which contains a sulfonamide moiety, and a chloropropyl chain, contributing to its potential biological activity. The presence of the chlorine atom may enhance the compound's reactivity and solubility in various solvents. This compound is likely to exhibit properties typical of boronic acids, such as the ability to participate in Suzuki coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the sulfamoyl group may impart specific pharmacological properties, potentially influencing its interaction with biological targets. Overall, [4-(3-chloropropylsulfamoyl)phenyl]boronic acid represents a versatile building block in chemical research and development.
Formula:C9H13BClNO4S
InChI:InChI=1/C9H13BClNO4S/c11-6-1-7-12-17(15,16)9-4-2-8(3-5-9)10(13)14/h2-5,12-14H,1,6-7H2
SMILES:C(CCl)CNS(=O)(=O)c1ccc(cc1)B(O)O
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