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CAS 1402238-32-7

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B-[4-(2-Fluorophenoxy)phenyl]boronic acid

Description:
B-[4-(2-Fluorophenoxy)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 applications, including organic synthesis and medicinal chemistry. The compound features a biphenyl structure with a fluorinated phenoxy group, which can influence its electronic properties and reactivity. The fluorine atom may enhance the compound's lipophilicity and alter its interaction with biological targets. Boronic acids are often utilized in Suzuki coupling reactions, a key method for forming carbon-carbon bonds in organic synthesis. Additionally, the presence of the boronic acid moiety allows for potential applications in drug development, particularly in the design of inhibitors for certain enzymes. The compound's solubility, stability, and reactivity can be influenced by factors such as pH and the presence of other functional groups. Overall, B-[4-(2-Fluorophenoxy)phenyl]boronic acid represents a versatile building block in both synthetic and medicinal chemistry.
Formula:C12H10BFO3
InChI:InChI=1S/C12H10BFO3/c14-11-3-1-2-4-12(11)17-10-7-5-9(6-8-10)13(15)16/h1-8,15-16H
InChI key:InChIKey=IQNYGJLCROJQSI-UHFFFAOYSA-N
SMILES:O(C1=CC=C(B(O)O)C=C1)C2=C(F)C=CC=C2
Synonyms:
  • Boronic acid, B-[4-(2-fluorophenoxy)phenyl]-
  • B-[4-(2-Fluorophenoxy)phenyl]boronic acid
  • [4-(2-Fluorophenoxy)phenyl]boronic acid
  • IQNYGJLCROJQSI-UHFFFAOYSA-N
  • 4-(2-Fluorophenoxy)phenylboronic acid
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