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CAS 871329-75-8

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B-[3-[(Methylamino)sulfonyl]phenyl]boronic acid

Description:
B-[3-[(Methylamino)sulfonyl]phenyl]boronic acid, with the CAS number 871329-75-8, is a boronic acid derivative characterized by the presence of a boron atom bonded to a phenyl group that is further substituted with a methylamino and sulfonyl functional group. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the presence of the sulfonamide group. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The methylamino group may impart basic characteristics, while the sulfonyl moiety can enhance the compound's reactivity and solubility. Additionally, this compound may exhibit biological activity, potentially serving as a pharmacophore in drug development. Its unique structure allows for interactions with biological targets, making it of interest in the fields of medicinal chemistry and biochemistry.
Formula:C7H10BNO4S
InChI:InChI=1S/C7H10BNO4S/c1-9-14(12,13)7-4-2-3-6(5-7)8(10)11/h2-5,9-11H,1H3
InChI key:InChIKey=IUSXOPNERIFVRV-UHFFFAOYSA-N
SMILES:S(NC)(=O)(=O)C1=CC(B(O)O)=CC=C1
Synonyms:
  • B-[3-[(Methylamino)sulfonyl]phenyl]boronic acid
  • Boronic acid, [3-[(methylamino)sulfonyl]phenyl]-
  • Boronicacid, [3-[(methylamino)sulfonyl]phenyl]- (9CI)
  • [3-(Methylaminosulfonyl)phenyl]boronic acid
  • [3-(Methylsulfamoyl)phenyl]boronic acid
  • [3-(Methylsulfamoyl)phenyl]boronicacid
  • [3-(N-Methylsulfamoyl)phenyl]boronic acid
  • Boronic acid, B-[3-[(methylamino)sulfonyl]phenyl]-
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