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CAS 259209-20-6

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(4-fluoro-2-hydroxyphenyl)boronic acid

Description:
(4-Fluoro-2-hydroxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenolic structure. This compound features a fluorine atom at the para position relative to the hydroxyl group on the aromatic ring, which can influence its reactivity and solubility. Typically, boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in various applications, including organic synthesis and medicinal chemistry. The hydroxyl group contributes to its acidity, allowing it to participate in reactions such as Suzuki coupling, which is essential for forming carbon-carbon bonds. Additionally, the presence of the fluorine atom can enhance the compound's electronic properties, potentially affecting its interactions in biological systems. Overall, (4-fluoro-2-hydroxyphenyl)boronic acid is a versatile compound with applications in drug development and materials science, owing to its unique structural features and reactivity.
Formula:C6H6BFO3
InChI:InChI=1/C6H6BFO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9-11H
SMILES:c1cc(c(cc1F)O)B(O)O
Synonyms:
  • boronic acid, B-(4-fluoro-2-hydroxyphenyl)-
  • 4-Fluoro-2-hydroxyphenylboronic acid
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