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CAS 128796-39-4

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4-(Trifluoromethyl)phenylboronic acid

Description:
4-(Trifluoromethyl)phenylboronic 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. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar organic solvents. The trifluoromethyl group enhances the compound's lipophilicity and can influence its reactivity and interaction with biological systems. As a boronic acid, it can participate in various chemical reactions, including Suzuki coupling, which is significant in organic synthesis for forming carbon-carbon bonds. Additionally, it can act as a Lewis acid, coordinating with bases and playing a role in catalysis. The presence of the trifluoromethyl group may also impart unique electronic properties, making it useful in the development of pharmaceuticals and agrochemicals. Overall, 4-(Trifluoromethyl)phenylboronic acid is a versatile compound with applications in synthetic chemistry and materials science.
Formula:C7H6BF3O2
InChI:InChI=1S/C7H6BF3O2/c9-7(10,11)5-1-3-6(4-2-5)8(12)13/h1-4,12-13H
InChI key:InChIKey=ALMFIOZYDASRRC-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=CC=C(B(O)O)C=C1
Synonyms:
  • 4-(Trifluoromethyl)Benzeneboronic Acid
  • 4-(Trifluoromethyl)Phenylboronic Acid
  • 4-[(Trifluoromethyl)-Phenyl]-Boronic Acid
  • B-[4-(Trifluoromethyl)phenyl]boronic acid
  • Boronic acid, B-[4-(trifluoromethyl)phenyl]-
  • Boronic acid, [4-(trifluoromethyl)phenyl]-
  • [p-(Trifluoromethyl)phenyl]boronic acid
  • p-(Trifluoromethyl) phenylboronic acid
  • α,α,α-Trifluoro-p-tolylboronic acid
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