CymitQuimica logo

CAS 351422-73-6

:

3-carbamoylphenylboronic acid

Description:
3-Carbamoylphenylboronic acid is an organic compound characterized by the presence of both a boronic acid functional group and a carbamoyl group attached to a phenyl ring. The boronic acid moiety is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The carbamoyl group contributes to the compound's potential as a building block in drug development, particularly in the design of inhibitors or ligands. This compound typically exhibits moderate solubility in polar solvents due to the presence of both polar functional groups. Its reactivity can be influenced by the pH of the environment, as boronic acids can exist in different forms depending on the protonation state. Additionally, 3-carbamoylphenylboronic acid may exhibit biological activity, making it of interest in pharmaceutical research. Overall, its unique structural features and functional groups provide a versatile platform for further chemical modifications and applications in various fields.
Formula:C7H8BNO3
InChI:InChI=1S/C7H8BNO3/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,11-12H,(H2,9,10)
InChI key:InChIKey=WDGWHKRJEBENCE-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(N)=O)=CC=C1
Synonyms:
  • (3-Aminocarbonylphenyl)boronic acid
  • (3-Carbamoylphenyl)Boronic Acid
  • 3-(Aminocarbonyl)phenylboronic acid
  • 3-Aminocarbonylpenylboronic Acid
  • 3-Carbamoylphenylboronic Acid
  • 3-Carboxamidephenylboronic acid
  • B-[3-(Aminocarbonyl)phenyl]boronic acid
  • Benzamide-3-Boronic Acid
  • Boronic acid, B-[3-(aminocarbonyl)phenyl]-
  • Boronic acid, [3-(aminocarbonyl)phenyl]-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.