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CAS 958451-79-1

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B-[4-(Difluoromethoxy)-3-(trifluoromethyl)phenyl]boronic acid

Description:
B-[4-(Difluoromethoxy)-3-(trifluoromethyl)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 and is widely used in organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with both a difluoromethoxy group and a trifluoromethyl group, contributing to its unique electronic properties and lipophilicity. The difluoromethoxy group enhances the compound's reactivity and solubility in organic solvents, while the trifluoromethyl group can influence its biological activity and stability. This compound is typically utilized in cross-coupling reactions, such as Suzuki-Miyaura coupling, making it valuable in the synthesis of complex organic molecules. Additionally, its boronic acid moiety allows for potential applications in drug development and materials science, particularly in the design of sensors and catalysts. Overall, the unique combination of functional groups in this compound provides a versatile platform for various chemical applications.
Formula:C8H6BF5O3
InChI:InChI=1S/C8H6BF5O3/c10-7(11)17-6-2-1-4(9(15)16)3-5(6)8(12,13)14/h1-3,7,15-16H
InChI key:InChIKey=NPFRNEQAEFRASI-UHFFFAOYSA-N
SMILES:O(C(F)F)C1=C(C(F)(F)F)C=C(B(O)O)C=C1
Synonyms:
  • Boronic acid, B-[4-(difluoromethoxy)-3-(trifluoromethyl)phenyl]-
  • B-[4-(Difluoromethoxy)-3-(trifluoromethyl)phenyl]boronic acid
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