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CAS 864759-67-1

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B-[3-Methyl-4-(trifluoromethyl)phenyl]boronic acid

Description:
B-[3-Methyl-4-(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 valuable in various chemical reactions, particularly in Suzuki coupling reactions. This 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, which can enhance the acidity of the boronic acid moiety. The presence of these substituents can also affect the compound's solubility, stability, and interaction with biological systems. B-[3-Methyl-4-(trifluoromethyl)phenyl]boronic acid is utilized in organic synthesis, medicinal chemistry, and materials science, particularly in the development of pharmaceuticals and agrochemicals. Its unique structural features make it a subject of interest for researchers exploring new synthetic methodologies and applications in drug discovery.
Formula:C8H8BF3O2
InChI:InChI=1S/C8H8BF3O2/c1-5-4-6(9(13)14)2-3-7(5)8(10,11)12/h2-4,13-14H,1H3
InChI key:InChIKey=WYIPXMTWQBAPEE-UHFFFAOYSA-N
SMILES:C(F)(F)(F)C1=C(C)C=C(B(O)O)C=C1
Synonyms:
  • 3-Methyl-4-trifluoromethylbenzeneboronic acid
  • B-[3-Methyl-4-(trifluoromethyl)phenyl]boronic acid
  • Boronic acid, [3-methyl-4-(trifluoromethyl)phenyl]-
  • boronic acid, B-[3-methyl-4-(trifluoromethyl)phenyl]-
  • (3-Methyl-4-(trifluoromethyl)phenyl)boronic acid
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