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CAS 881402-22-8

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[2-fluoro-5-(trifluoromethoxy)phenyl]boronic acid

Description:
[2-Fluoro-5-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that contains both a fluorine atom and a trifluoromethoxy group. This compound typically exhibits properties such as high reactivity due to the boronic acid moiety, which can participate in various chemical reactions, including Suzuki coupling, a key reaction in organic synthesis. The presence of the trifluoromethoxy group enhances its lipophilicity and may influence its electronic properties, making it useful in medicinal chemistry and materials science. Additionally, the fluorine substituents can impart unique characteristics such as increased stability and altered solubility in different solvents. The compound is likely to be solid at room temperature and may require careful handling due to its reactive nature. Its applications may extend to pharmaceuticals, agrochemicals, and as a building block in the synthesis of more complex molecules.
Formula:C7H5BF4O3
InChI:InChI=1/C7H5BF4O3/c9-6-2-1-4(15-7(10,11)12)3-5(6)8(13)14/h1-3,13-14H
SMILES:c1cc(c(cc1OC(F)(F)F)B(O)O)F
Synonyms:
  • boronic acid, B-[2-fluoro-5-(trifluoromethoxy)phenyl]-
  • [2-Fluoro-5-(trifluoromethoxy)phenyl]boronic acid
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