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CAS 958451-71-3

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B-[2-(Difluoromethoxy)-5-fluorophenyl]boronic acid

Description:
B-[2-(Difluoromethoxy)-5-fluorophenyl]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 both difluoromethoxy and fluorine groups, which can influence its reactivity and solubility. The difluoromethoxy group enhances the compound's electronic properties, potentially increasing its reactivity in organic synthesis. Additionally, the presence of fluorine atoms can impart unique characteristics such as increased lipophilicity and altered biological activity. This compound is typically utilized in medicinal chemistry and materials science, where boronic acids play a crucial role in the development of pharmaceuticals and advanced materials. Its specific properties, such as melting point, solubility, and stability, would depend on the molecular structure and the surrounding environment. Overall, B-[2-(Difluoromethoxy)-5-fluorophenyl]boronic acid is a valuable compound in synthetic organic chemistry.
Formula:C7H6BF3O3
InChI:InChI=1S/C7H6BF3O3/c9-4-1-2-6(14-7(10)11)5(3-4)8(12)13/h1-3,7,12-13H
InChI key:InChIKey=OJLMHKHBIZUECP-UHFFFAOYSA-N
SMILES:O(C(F)F)C1=C(B(O)O)C=C(F)C=C1
Synonyms:
  • 3-(Difluoromethoxy)-5-fluorophenylboronic acid
  • B-[2-(Difluoromethoxy)-5-fluorophenyl]boronic acid
  • Boronic acid, B-[2-(difluoromethoxy)-5-fluorophenyl]-
  • [2-(Difluoromethoxy)-5-fluorophenyl]boronic acid
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