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CAS 957061-11-9

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[2-chloro-3-(trifluoromethyl)phenyl]boronic acid

Description:
[2-Chloro-3-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a chlorine atom and a trifluoromethyl 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 and other cross-coupling reactions, making it valuable in organic synthesis and medicinal chemistry. The presence of the trifluoromethyl group enhances its lipophilicity and can influence biological activity, while the chlorine atom may affect the electronic properties of the aromatic system. In terms of solubility, boronic acids generally have moderate solubility in polar solvents, and the specific substituents can further influence this property. Overall, [2-chloro-3-(trifluoromethyl)phenyl]boronic acid is a versatile compound with applications in the development of pharmaceuticals and agrochemicals, as well as in materials science.
Formula:C7H5BClF3O2
InChI:InChI=1/C7H5BClF3O2/c9-6-4(7(10,11)12)2-1-3-5(6)8(13)14/h1-3,13-14H
SMILES:c1cc(c(c(c1)B(O)O)Cl)C(F)(F)F
Synonyms:
  • boronic acid, B-[2-chloro-3-(trifluoromethyl)phenyl]-
  • 2-Chloro-3-Trifluoromethylphenylboronic Acid
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