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CAS 871125-82-5

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B-[4-[(4-Fluorophenyl)methoxy]phenyl]boronic acid

Description:
B-[4-[(4-Fluorophenyl)methoxy]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. This compound features a phenyl ring substituted with a methoxy group and a fluorophenyl moiety, contributing to its unique electronic and steric properties. The fluorine atom enhances the compound's lipophilicity and may influence its reactivity and interaction with biological targets. Boronic acids are often utilized in organic synthesis, particularly in Suzuki coupling reactions, and can serve as important intermediates in the development of pharmaceuticals. The presence of the boronic acid group also allows for potential applications in sensor technology and materials science. Additionally, the compound's solubility and stability in various solvents can vary, which is crucial for its practical applications. Overall, B-[4-[(4-Fluorophenyl)methoxy]phenyl]boronic acid exemplifies the versatility of boron-containing compounds in both synthetic and medicinal chemistry.
Formula:C13H12BFO3
InChI:InChI=1S/C13H12BFO3/c15-12-5-1-10(2-6-12)9-18-13-7-3-11(4-8-13)14(16)17/h1-8,16-17H,9H2
InChI key:InChIKey=HNQLLMVLGZJPJT-UHFFFAOYSA-N
SMILES:O(CC1=CC=C(F)C=C1)C2=CC=C(B(O)O)C=C2
Synonyms:
  • B-[4-[(4-Fluorophenyl)methoxy]phenyl]boronic acid
  • Boronic acid, [4-[(4-fluorophenyl)methoxy]phenyl]-
  • [4-(4-Fluorobenzyloxy)phenyl]boronic acid
  • Boronic acid, B-[4-[(4-fluorophenyl)methoxy]phenyl]-
  • [4-[(4-Fluorophenyl)methoxy]phenyl]boronic acid
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