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CAS 178432-25-2

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2-(N,N-Dimethylsulphamoyl)phenylboronic acid

Description:
2-(N,N-Dimethylsulphamoyl)phenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a dimethylsulphamoyl group. This compound typically exhibits properties such as being a white to off-white solid, with solubility in polar solvents like water and methanol, which is common for boronic acids due to their ability to form hydrogen bonds. The presence of the boronic acid moiety allows for participation in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and medicinal chemistry. Additionally, the dimethylsulphamoyl group enhances its solubility and may influence its biological activity, potentially serving as a pharmacophore in drug design. The compound's reactivity and functionalization capabilities make it a useful intermediate in the synthesis of more complex molecules, particularly in the development of pharmaceuticals and agrochemicals. Safety data should be consulted for handling and storage, as with all chemical substances.
Formula:C5H4Cl2N2
InChI:InChI=1/C5H4Cl2N2/c6-4-1-3(8)2-9-5(4)7/h1-2H,8H2
SMILES:c1c(cnc(c1Cl)Cl)N
Synonyms:
  • O-[(Dimethylamino)Sulfonyl]Phenylboronic Acid
  • 2-(N,N-Dimethylsulfamoyl)Phenylboronic Acid
  • 2-(N,N-Dimethylsulphamoyl)Benzeneboronic Acid
  • Akos Brn-0039
  • {2-[(Dimethylamino)Sulfonyl]Phenyl}Boronicacid
  • 2-Dimethylsulfamoyl-benzeneboronic acid
  • N,N-Dimethyl 2-boronobenzenesulfonamide
  • 2-(N,N-Dimethylsulphonyl)Benzeneboronic Acid
  • 2-(N,N-diMethylsulfonyl) Phenylboronic acid
  • [2-(Dimethylsulfamoyl)Phenyl]Boronic Acid
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