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CAS 196083-18-8

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2,5-BIS(TRIFLUOROMETHYL)BENZENEBORONIC ACID

Description:
2,5-Bis(trifluoromethyl)benzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring that has two trifluoromethyl substituents at the 2 and 5 positions. This compound typically exhibits high reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling, making it valuable in organic synthesis and materials science. The trifluoromethyl groups contribute to the compound's lipophilicity and can influence its electronic properties, enhancing its utility in medicinal chemistry and agrochemicals. Additionally, the presence of fluorine atoms often imparts unique characteristics such as increased stability and altered solubility in organic solvents. The compound is generally handled with care due to its potential reactivity and the toxicity associated with trifluoromethyl groups. Overall, 2,5-bis(trifluoromethyl)benzeneboronic acid is a significant compound in the field of synthetic organic chemistry, particularly in the development of complex molecular architectures.
Formula:C8H5BF6O2
InChI:InChI=1/C8H5BF6O2/c10-7(11,12)4-1-2-5(8(13,14)15)6(3-4)9(16)17/h1-3,16-17H
SMILES:c1cc(c(cc1C(F)(F)F)B(O)O)C(F)(F)F
Synonyms:
  • 2,5-Bis(Trifluoromethyl)Phenylboronic Acid
  • 2,5-Di(Trifluoromethyl)Phenyl Boronic Acid
  • 2,5-Bis(Trifluoromethyl)-Benzeneboronic Acid, 97+%
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