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CAS 913835-96-8

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[4-[isopropyl-[(4-methoxyphenyl)methyl]sulfamoyl]phenyl]boronic acid

Description:
[4-[isopropyl-[(4-methoxyphenyl)methyl]sulfamoyl]phenyl]boronic acid, with CAS number 913835-96-8, is a boronic acid derivative characterized by its unique structural features. This compound contains a boron atom bonded to a phenyl group, which is further substituted with a sulfamoyl group and an isopropyl moiety. The presence of the methoxyphenyl group enhances its lipophilicity, potentially influencing its biological activity. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including medicinal chemistry and organic synthesis. This specific compound may exhibit properties such as enzyme inhibition or modulation of biological pathways, particularly in the context of drug development. Its sulfonamide functionality suggests potential interactions with biological targets, which could be relevant in therapeutic contexts. Overall, the compound's structural complexity and functional groups contribute to its potential utility in research and pharmaceutical applications.
Formula:C17H22BNO5S
InChI:InChI=1/C17H22BNO5S/c1-13(2)19(12-14-4-8-16(24-3)9-5-14)25(22,23)17-10-6-15(7-11-17)18(20)21/h4-11,13,20-21H,12H2,1-3H3
SMILES:CC(C)N(Cc1ccc(cc1)OC)S(=O)(=O)c1ccc(cc1)B(O)O
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