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CAS 850033-39-5

:

[2-methyl-4-(trifluoromethoxy)phenyl]boronic acid

Description:
[2-Methyl-4-(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. This compound features a phenyl ring substituted with a methyl group and a trifluoromethoxy group, which enhances its reactivity and solubility in organic solvents. The trifluoromethoxy group contributes to the compound's unique electronic properties, making it useful in various applications, including medicinal chemistry and materials science. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of fluorine atoms can influence the compound's lipophilicity and biological activity. Overall, [2-methyl-4-(trifluoromethoxy)phenyl]boronic acid is a versatile compound with potential applications in drug development and synthetic organic chemistry, owing to its distinctive structural features and reactivity.
Formula:C8H8BF3O3
InChI:InChI=1/C8H8BF3O3/c1-5-4-6(15-8(10,11)12)2-3-7(5)9(13)14/h2-4,13-14H,1H3
SMILES:Cc1cc(ccc1B(O)O)OC(F)(F)F
Synonyms:
  • boronic acid, B-[2-methyl-4-(trifluoromethoxy)phenyl]-
  • [2-Methyl-4-(trifluoromethoxy)phenyl]boronic acid
  • 2-Methyl-4-(trifluoromethoxy)benzeneboronic acid 98%
  • 2-Methyl-4-(trifluoromethoxy)benzeneboronic acid
  • 2-Methyl-4-trifluoromethoxyphenylboronic acid
  • 2-Methyl-4-(trifluoromethoxy)phenylboronic acid
  • 2-Methyl-4-(trifluoromethoxy)benzeneboronicacid98%
  • 2-Methyl-4-(trifluoromethoxy)benzeneboronic
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