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CAS 913836-05-2

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[3-[(4-methoxyphenyl)methylsulfamoyl]phenyl]boronic acid

Description:
[3-[(4-methoxyphenyl)methylsulfamoyl]phenyl]boronic acid, with the CAS number 913836-05-2, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group and a sulfonamide moiety. This compound typically exhibits properties such as moderate solubility in polar organic solvents and potential reactivity with diols, making it useful in various organic synthesis applications, particularly in the formation of boronate esters. The presence of the methoxyphenyl group enhances its lipophilicity, which can influence its biological activity and interaction with target molecules. Additionally, boronic acids are known for their ability to form reversible covalent bonds with certain biomolecules, which can be exploited in drug design and development. The compound may also exhibit specific biological activities, including potential anti-cancer properties, due to its structural features. Overall, this compound represents a versatile building block in medicinal chemistry and materials science.
Formula:C14H16BNO5S
InChI:InChI=1/C14H16BNO5S/c1-21-13-7-5-11(6-8-13)10-16-22(19,20)14-4-2-3-12(9-14)15(17)18/h2-9,16-18H,10H2,1H3
SMILES:COc1ccc(cc1)CNS(=O)(=O)c1cccc(c1)B(O)O
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