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CAS 2055539-69-8

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3-Difluoromethoxy-5-fluoro-benzeneboronic acid

Description:
3-Difluoromethoxy-5-fluoro-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 benzene ring substituted with both difluoromethoxy and fluoro groups, contributing to its unique chemical properties. The difluoromethoxy group enhances the compound's lipophilicity and may influence its electronic properties, while the fluoro substituent can affect its reactivity and stability. As a boronic acid, it can participate in Suzuki coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The presence of fluorine atoms typically increases the compound's stability and can also modify its solubility in different solvents. Overall, 3-Difluoromethoxy-5-fluoro-benzeneboronic acid is a versatile compound with potential applications in pharmaceuticals and materials science, particularly in the development of new synthetic methodologies.
Formula:C7H6BF3O3
Synonyms:
  • 3-(Difluoromethoxy)-5-fluorophenylboronic acid
  • (3-(difluoromethoxy)-5-fluorophenyl)boronic acid
  • Boronic acid, B-[3-(difluoromethoxy)-5-fluorophenyl]-
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