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CAS 871126-17-9

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2-Fluoro-3-methoxy-6-bromophenylboronic acid

Description:
2-Fluoro-3-methoxy-6-bromophenylboronic 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. This compound features a phenyl ring substituted with a fluorine atom, a methoxy group, and a bromine atom, contributing to its unique reactivity and properties. The presence of the boronic acid group allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as well as in materials science for the synthesis of complex organic structures. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents. Its reactivity can be influenced by the electron-withdrawing and electron-donating effects of the substituents on the aromatic ring, which can affect its behavior in chemical reactions. Safety and handling precautions should be observed, as with all chemical substances, to mitigate any potential hazards.
Formula:C7H7BBrFO3
Synonyms:
  • 6-Bromo-2-fluoro-3-methoxybenzeneboronic acid
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