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CAS 913835-50-4

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[3-(3-chloropropylsulfonylamino)phenyl]boronic acid

Description:
[3-(3-Chloropropylsulfonylamino)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a sulfonamide group and a chloropropyl moiety, which can enhance its reactivity and solubility in organic solvents. The presence of the chloropropylsulfonylamino group may impart specific biological activity, potentially making it relevant in medicinal chemistry. Additionally, boronic acids are often utilized in the development of sensors and in the synthesis of complex organic molecules. The compound's structure suggests it may exhibit polar characteristics due to the sulfonamide and boronic acid functionalities, influencing its interactions in biological systems and its solubility in various solvents. Overall, [3-(3-chloropropylsulfonylamino)phenyl]boronic acid is a versatile compound with potential applications in organic synthesis and pharmaceuticals.
Formula:C9H13BClNO4S
InChI:InChI=1/C9H13BClNO4S/c11-5-2-6-17(15,16)12-9-4-1-3-8(7-9)10(13)14/h1,3-4,7,12-14H,2,5-6H2
SMILES:c1cc(cc(c1)NS(=O)(=O)CCCCl)B(O)O
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