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CAS 881402-25-1

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[2-Fluoro-3-(trifluoromethoxy)phenyl]boronic acid

Description:
[2-Fluoro-3-(trifluoromethoxy)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it valuable in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a trifluoromethoxy group, which enhances its reactivity and solubility in various organic solvents. The trifluoromethoxy group contributes to the compound's unique electronic properties, potentially influencing its interactions in chemical reactions. As a boronic acid, it can participate in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds. The presence of fluorine atoms typically increases the lipophilicity and stability of the compound, making it of interest in drug development and material science. Overall, [2-Fluoro-3-(trifluoromethoxy)phenyl]boronic acid is a versatile building block in synthetic chemistry, with applications ranging from pharmaceuticals to advanced materials.
Formula:C7H5BF4O3
InChI:InChI=1/C7H5BF4O3/c9-6-4(8(13)14)2-1-3-5(6)15-7(10,11)12/h1-3,13-14H
SMILES:c1cc(c(c(c1)OC(F)(F)F)F)B(O)O
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