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CAS 947533-86-0

:

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

Description:
[2-Methyl-3-(trifluoromethyl)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 useful in various chemical reactions, particularly in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with both a methyl group and a trifluoromethyl group, which can influence its electronic properties and reactivity. The trifluoromethyl group is known for its electron-withdrawing effects, enhancing the acidity of the boronic acid moiety. This compound is typically used in cross-coupling reactions, such as Suzuki-Miyaura coupling, to form carbon-carbon bonds. Additionally, its unique substituents may impart specific biological activities or enhance solubility in certain solvents. Overall, [2-methyl-3-(trifluoromethyl)phenyl]boronic acid is a versatile building block in synthetic organic chemistry, with applications in pharmaceuticals and materials science.
Formula:C8H8BF3O2
InChI:InChI=1/C8H8BF3O2/c1-5-6(8(10,11)12)3-2-4-7(5)9(13)14/h2-4,13-14H,1H3
SMILES:Cc1c(cccc1B(O)O)C(F)(F)F
Synonyms:
  • boronic acid, B-[2-methyl-3-(trifluoromethyl)phenyl]-
  • [2-Methyl-3-(trifluoromethyl)phenyl]boronic acid
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