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CAS 756520-78-2

:

B-[2-[(Methylsulfonyl)amino]phenyl]boronic acid

Description:
B-[2-[(Methylsulfonyl)amino]phenyl]boronic acid, with the CAS number 756520-78-2, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a methylsulfonylamino group. 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 medicinal chemistry and organic synthesis. The methylsulfonyl group enhances its solubility in polar solvents and may influence its biological activity. Additionally, boronic acids are known for their role in the Suzuki coupling reaction, a key method for forming carbon-carbon bonds in organic synthesis. The compound's structure suggests potential applications in drug development, particularly in targeting specific biological pathways or as a tool in chemical biology. Its stability, reactivity, and solubility characteristics are essential for its functionality in both laboratory and therapeutic contexts.
Formula:C7H10BNO4S
InChI:InChI=1/C7H10BNO4S/c1-14(12,13)9-7-5-3-2-4-6(7)8(10)11/h2-5,9-11H,1H3
InChI key:InChIKey=RPRMOEFOTPSWBO-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(NS(C)(=O)=O)C=CC=C1
Synonyms:
  • (2-(Methylsulfonamido)phenyl)boronic acid
  • 2-(Methylsulfonylamino)benzeneboronic acid
  • 2-Methanesulfonylaminophenylboronic acid
  • B-[2-[(Methylsulfonyl)amino]phenyl]boronic acid
  • Boronic acid, [2-[(methylsulfonyl)amino]phenyl]-
  • boronic acid, B-[2-[(methylsulfonyl)amino]phenyl]-
  • {2-[(Methylsulfonyl)amino]phenyl}boronic acid
  • 2-(METHYLSULFONYLAMINO)PHENYLBORONIC ACID
  • 2-N-(METHANESULFONAMIDE)PHENYLBORONIC ACID
  • [(2-METHYLSULPHONYL)AMINOPHENYL]BORONIC ACID
  • See more synonyms
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