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CAS 503309-11-3

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2-Fluoro-4-(trifluoromethyl)benzeneboronic acid

Description:
2-Fluoro-4-(trifluoromethyl)benzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a fluorinated aromatic ring. The molecular structure features a fluorine atom at the ortho position and a trifluoromethyl group at the para position relative to the boronic acid group on a benzene ring. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable for forming carbon-carbon bonds. The presence of multiple fluorine atoms enhances its lipophilicity and can influence its reactivity and solubility in various solvents. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in various applications, including drug development and materials science. The compound's unique electronic and steric properties, derived from its fluorinated substituents, contribute to its utility in synthetic chemistry and potential applications in pharmaceuticals.
Formula:C7H5BF4O2
InChI:InChI=1/C7H5BF4O2/c9-6-3-4(7(10,11)12)1-2-5(6)8(13)14/h1-3,13-14H
SMILES:c1cc(c(cc1C(F)(F)F)F)B(O)O
Synonyms:
  • 2-Fluoro-4-(Trifluoromethyl)Phenylboronic Acid
  • (2,2,2-Trifluoroethyl)Hydrazine
  • 2-Fluoro-4-(trifluoromethyl)benzeneboronicacid
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