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CAS 1072944-17-2

:

B-[2-Hydroxy-3-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-Hydroxy-3-(trifluoromethyl)phenyl]boronic acid, identified by its CAS number 1072944-17-2, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features a hydroxyl group and a trifluoromethyl substituent. This compound typically exhibits properties such as high solubility in polar solvents, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The trifluoromethyl group enhances the compound's electronic properties, potentially increasing its reactivity and stability. Additionally, the hydroxyl group contributes to its acidity, allowing it to participate in various acid-base reactions. B-[2-Hydroxy-3-(trifluoromethyl)phenyl]boronic acid is of interest in medicinal chemistry and materials science due to its potential applications in drug development and the synthesis of functionalized materials. Its unique structural features make it a valuable building block in the synthesis of more complex organic molecules.
Formula:C7H6BF3O3
InChI:InChI=1S/C7H6BF3O3/c9-7(10,11)4-2-1-3-5(6(4)12)8(13)14/h1-3,12-14H
InChI key:InChIKey=PDKFKKGOOLKAGR-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(O)C(B(O)O)=CC=C1
Synonyms:
  • Boronic acid, B-[2-hydroxy-3-(trifluoromethyl)phenyl]-
  • B-[2-Hydroxy-3-(trifluoromethyl)phenyl]boronic acid
  • 2-Hydroxy-3-(trifluoromethyl)phenylboronic acid
  • [2-Hydroxy-3-(trifluoromethyl)phenyl]boronic acid
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