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CAS 957061-16-4

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B-[2-[(Diethylamino)sulfonyl]phenyl]boronic acid

Description:
B-[2-[(Diethylamino)sulfonyl]phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a diethylamino sulfonyl group, which enhances its solubility and reactivity. The presence of the boronic acid moiety allows for participation in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds. Additionally, the diethylamino group can influence the electronic properties of the molecule, potentially affecting its reactivity and interaction with biological targets. This compound may be utilized in the development of pharmaceuticals, particularly in the design of inhibitors or modulators of biological pathways. Its unique structure and functional groups make it a valuable tool in both synthetic and medicinal chemistry.
Formula:C10H16BNO4S
InChI:InChI=1/C10H16BNO4S/c1-3-12(4-2)17(15,16)10-8-6-5-7-9(10)11(13)14/h5-8,13-14H,3-4H2,1-2H3
InChI key:InChIKey=DJGWUWODZFKVIY-UHFFFAOYSA-N
SMILES:S(N(CC)CC)(=O)(=O)C1=C(B(O)O)C=CC=C1
Synonyms:
  • B-[2-[(Diethylamino)sulfonyl]phenyl]boronic acid
  • boronic acid, B-[2-[(diethylamino)sulfonyl]phenyl]-
  • [2-(Diethylsulfamoyl)phenyl]boronic acid
  • N,N-Diethyl 2-boronobenzenesulfonamide
  • 2-(N,N-diethylsulfamoyl)phenylboronic acid USP/EP/BP
  • 2-N,N-Diethylsulfamoylphenylboronic acid
  • 2-N,N-DiethyL
  • 2-(N,N-diethylsulfamoyl)phenylboronic acid
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