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CAS 871329-77-0

:

B-[3-[[(1-Methylethyl)amino]sulfonyl]phenyl]boronic acid

Description:
B-[3-[[(1-Methylethyl)amino]sulfonyl]phenyl]boronic acid, identified by its CAS number 871329-77-0, 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 associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The sulfonamide group contributes to its solubility and reactivity, enhancing its potential as a pharmacophore in drug design. Additionally, the presence of the isopropylamino group may influence its biological activity and interaction with target proteins. Overall, this compound is of interest in research areas focused on enzyme inhibition and the development of therapeutic agents, particularly in the context of diseases where boronic acids have shown promise, such as cancer and diabetes. Its unique structural features allow for specific interactions in biological systems, making it a valuable compound in chemical and pharmaceutical research.
Formula:C9H14BNO4S
InChI:InChI=1S/C9H14BNO4S/c1-7(2)11-16(14,15)9-5-3-4-8(6-9)10(12)13/h3-7,11-13H,1-2H3
InChI key:InChIKey=KCJMBNYQVZPTRG-UHFFFAOYSA-N
SMILES:S(NC(C)C)(=O)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • 3-(Isopropylaminosulfonyl)phenylboronic acid
  • B-[3-[[(1-Methylethyl)amino]sulfonyl]phenyl]boronic acid
  • Boronic acid, [3-[[(1-methylethyl)amino]sulfonyl]phenyl]-
  • Boronicacid, [3-[[(1-methylethyl)amino]sulfonyl]phenyl]- (9CI)
  • [3-(N-Isopropylsulfamoyl)phenyl]boronic acid
  • [3-[(Propan-2-yl)sulfamoyl]phenyl]boronic acid
  • Boronic acid, B-[3-[[(1-methylethyl)amino]sulfonyl]phenyl]-
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