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CAS 1423-27-4

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2-Trifluoromethylphenylboronic acid

Description:
2-Trifluoromethylphenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has a trifluoromethyl substituent in the ortho position. This compound typically appears as a white to off-white solid and is known for its utility in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and selectivity in various chemical reactions. Additionally, the boronic acid moiety allows for the formation of stable complexes with diols, making it useful in the development of sensors and in medicinal chemistry for drug design. Its properties, such as solubility and stability, can vary depending on the solvent and conditions used. Safety precautions should be taken when handling this compound, as with many organoboron compounds, due to potential reactivity and toxicity.
Formula:C7H6BF3O2
InChI:InChI=1S/C7H6BF3O2/c9-7(10,11)5-3-1-2-4-6(5)8(12)13/h1-4,12-13H
InChI key:InChIKey=JNSBEPKGFVENFS-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(B(O)O)C=CC=C1
Synonyms:
  • 2-(Trifluoromethyl)phenylboronic acid
  • 2-Trifluoromethylbenzeneboronic acid
  • 2-[(Trifluoromethyl)-Benzene]-Boronic Acid
  • B-[2-(Trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[2-(trifluoromethyl)phenyl]-
  • Boronic acid, [2-(trifluoromethyl)phenyl]-
  • o-Tolueneboronic acid, α,α,α-trifluoro-
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