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CAS 139301-27-2

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4-(Trifluoromethoxy)benzeneboronic acid

Description:
4-(Trifluoromethoxy)benzeneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a benzene ring that is further substituted with a trifluoromethoxy group. This compound typically exhibits a white to off-white solid appearance and is soluble in polar organic solvents. The trifluoromethoxy group enhances its reactivity and polarity, making it useful in various chemical reactions, particularly in Suzuki coupling reactions, which are pivotal in organic synthesis for forming carbon-carbon bonds. The boronic acid moiety allows for the formation of stable complexes with diols, which is advantageous in applications such as drug development and materials science. Additionally, the presence of fluorine atoms contributes to its unique electronic properties, potentially influencing its reactivity and interaction with biological systems. Overall, 4-(Trifluoromethoxy)benzeneboronic acid is a valuable compound in synthetic organic chemistry, particularly in the development of pharmaceuticals and advanced materials.
Formula:C7H6BF3O3
InChI:InChI=1/C7H6BF3O3/c9-7(10,11)14-6-3-1-5(2-4-6)8(12)13/h1-4,12-13H
SMILES:c1cc(ccc1B(O)O)OC(F)(F)F
Synonyms:
  • 4-(Trifluoromethoxy)Phenylboronic Acid
  • P-Trifluoromethoxy Benzoboric Acid
  • P-(Trifluoromethoxy)Phenylboronic Acid
  • 4-(Trifluoromethoxy)phenylboronicacid(containsvaryingamountsofanhydride)
  • 4-(Trifluoromethoxy)phenylboronic aicd
  • 4-Trifluoromethoxyphenylboronic acid
  • 4-[(Trifluoromethoxy)-Phenyl]-Boronic Acid
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