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CAS 1451393-39-7

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B-[3-Formyl-5-(trifluoromethoxy)phenyl]boronic acid

Description:
B-[3-Formyl-5-(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 chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a formyl group and a trifluoromethoxy group, which can influence its reactivity and solubility. The trifluoromethoxy group is notable for its electron-withdrawing properties, which can enhance the electrophilicity of the carbonyl carbon in the formyl group. This compound may exhibit unique properties such as potential applications in organic synthesis, medicinal chemistry, and materials science. Additionally, its boronic acid functionality allows for participation in cross-coupling reactions, making it valuable in the development of complex organic molecules. As with many organoboron compounds, it may also exhibit specific solubility characteristics in various solvents, which can be important for its application in laboratory settings.
Formula:C8H6BF3O4
InChI:InChI=1S/C8H6BF3O4/c10-8(11,12)16-7-2-5(4-13)1-6(3-7)9(14)15/h1-4,14-15H
InChI key:InChIKey=ISVJXSCLOFBOHL-UHFFFAOYSA-N
SMILES:O(C(F)(F)F)C1=CC(B(O)O)=CC(C=O)=C1
Synonyms:
  • B-[3-Formyl-5-(trifluoromethoxy)phenyl]boronic acid
  • Boronic acid, B-[3-formyl-5-(trifluoromethoxy)phenyl]-
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