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CAS 947533-09-7

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3-Fluoro-4-(2,2,2-trifluoro-ethoxy)-benzeneboronic acid

Description:
3-Fluoro-4-(2,2,2-trifluoro-ethoxy)-benzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in forming covalent bonds with various nucleophiles. This compound features a fluorinated aromatic ring, which enhances its electronic properties and can influence its reactivity and solubility. The trifluoroethoxy group contributes to its lipophilicity and may affect its interaction with biological systems. The presence of fluorine atoms typically increases the compound's stability and can alter its physical properties, such as boiling and melting points. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, making this compound potentially valuable in the development of pharmaceuticals and agrochemicals. Additionally, the unique combination of functional groups may impart specific characteristics that could be exploited in material science or medicinal chemistry. As with many fluorinated compounds, considerations regarding environmental impact and toxicity are essential in its application and handling.
Formula:C8H7BF4O3
Synonyms:
  • Boronic acid, B-[3-fluoro-4-(2,2,2-trifluoroethoxy)phenyl]-
  • 3-Fluoro-4-(2,2,2-trifluoroethoxy)benzeneboronicacid98%
  • 4-Borono-beta,beta,beta,2-tetrafluorophenetole
  • 3-Fluoro-4-(2,2,2-trifluoroethoxy)phenylboronic acid
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