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CAS 212837-49-5

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2,3-Difluoro-4-propoxylphenylboronic acid

Description:
2,3-Difluoro-4-propoxylphenylboronic 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 phenyl ring substituted with two fluorine atoms at the 2 and 3 positions, enhancing its electronic properties and potentially influencing its reactivity. The presence of a propoxy group at the 4-position contributes to its solubility and steric properties. This compound is typically a solid at room temperature and may exhibit moderate stability under standard conditions, although it can be sensitive to moisture due to the boronic acid moiety. Its unique structure allows for potential applications in drug development, particularly in the design of inhibitors or ligands that interact with biological targets. As with many boronic acids, it may also be involved in cross-coupling reactions, making it valuable in synthetic organic chemistry.
Formula:C9H11BF2O3
Synonyms:
  • (2,3-difluoro-4-propoxyphenyl)Boronic acid
  • 2,3-Difluoro-4-propoxyphenylboronic acid
  • 2,3-Difluoro-4-propoxybenzeneboronic acid
  • 2,3-Difluoro-4-n-propoxybenzeneboronic acid
  • 2,3-Difluoro-4-Propyloxyphenylboric Acid
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