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CAS 1204580-94-8

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B-[2-Formyl-5-(trifluoromethyl)phenyl]boronic acid

Description:
B-[2-Formyl-5-(trifluoromethyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its reactivity in various organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a formyl group (-CHO) and a trifluoromethyl group (-CF3), which significantly influences its electronic properties and reactivity. The trifluoromethyl group is highly electronegative, imparting unique characteristics such as increased lipophilicity and potential for enhanced biological activity. The presence of the formyl group allows for further functionalization, making it a versatile intermediate in organic synthesis. Additionally, boronic acids are known for their ability to form reversible complexes with diols, which can be exploited in sensor applications and drug design. Overall, this compound's structural features suggest potential utility in medicinal chemistry and materials science, particularly in the development of new pharmaceuticals or advanced materials.
Formula:C8H6BF3O3
InChI:InChI=1S/C8H6BF3O3/c10-8(11,12)6-2-1-5(4-13)7(3-6)9(14)15/h1-4,14-15H
InChI key:InChIKey=MUEODBDFMVYZAC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(C=O)C=CC(C(F)(F)F)=C1
Synonyms:
  • B-[2-Formyl-5-(trifluoromethyl)phenyl]boronic acid
  • 2-Formyl-5-(trifluoromethyl)phenylboronic acid
  • Boronic acid, B-[2-formyl-5-(trifluoromethyl)phenyl]-
  • [2-Formyl-5-(trifluoromethyl)phenyl]boronic acid
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