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CAS 957034-62-7

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[4-fluoro-3-(2,2,2-trifluoroethoxy)phenyl]boronic acid

Description:
[4-Fluoro-3-(2,2,2-trifluoroethoxy)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. This compound features a phenyl ring substituted with a fluorine atom and an ether group containing trifluoroethyl moieties, contributing to its unique chemical properties. The trifluoroethoxy group enhances the lipophilicity and stability of the compound, making it potentially useful in various applications, including medicinal chemistry and materials science. The boronic acid functionality allows for participation in Suzuki coupling reactions, which are valuable in the synthesis of complex organic molecules. Additionally, the presence of fluorine atoms can influence the electronic properties and reactivity of the compound, potentially enhancing its biological activity. Overall, [4-fluoro-3-(2,2,2-trifluoroethoxy)phenyl]boronic acid is a versatile compound with significant implications in synthetic organic chemistry and drug development.
Formula:C8H7BF4O3
InChI:InChI=1/C8H7BF4O3/c10-6-2-1-5(9(14)15)3-7(6)16-4-8(11,12)13/h1-3,14-15H,4H2
SMILES:c1cc(c(cc1B(O)O)OCC(F)(F)F)F
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