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CAS 187804-79-1

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[3-fluoro-4-(trifluoromethoxy)phenyl]boronic acid

Description:
[3-Fluoro-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, making it useful in various applications such as organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a fluorine atom and a trifluoromethoxy group, which enhances its reactivity and solubility in organic solvents. The trifluoromethoxy group contributes to the compound's unique electronic properties, potentially influencing its behavior in chemical reactions. Additionally, boronic acids are often utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. The presence of fluorine atoms typically increases the lipophilicity and stability of the compound, making it a candidate for pharmaceutical development. Overall, [3-fluoro-4-(trifluoromethoxy)phenyl]boronic acid exhibits distinctive chemical properties that are valuable in synthetic organic chemistry and drug discovery.
Formula:C7H5BF4O3
InChI:InChI=1/C7H5BF4O3/c9-5-3-4(8(13)14)1-2-6(5)15-7(10,11)12/h1-3,13-14H
SMILES:c1cc(c(cc1B(O)O)F)OC(F)(F)F
Synonyms:
  • Boronic acid, B-[3-fluoro-4-(trifluoromethoxy)phenyl]-
  • [3-FLUORO-4-(TRIFLUOROMETHOXY)PHENYL]BORONIC ACID
  • 3-FLUORO-4-(TRIFLUOROMETHOXY)BENZENEBORONIC ACID
  • See more synonyms
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