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CAS 1451393-19-3

:

2,3-Difluoro-6-benzyloxyphenylboronic acid

Description:
2,3-Difluoro-6-benzyloxyphenylboronic 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 benzyloxy group at the 6 position contributes to its lipophilicity and may affect its solubility and interaction with biological targets. As a boronic acid, it can participate in Suzuki-Miyaura cross-coupling reactions, making it valuable in the synthesis of complex organic molecules. Additionally, the fluorine substituents can impart unique characteristics such as increased metabolic stability and altered pharmacokinetics in drug development. Overall, 2,3-Difluoro-6-benzyloxyphenylboronic acid is a versatile compound with significant implications in both synthetic and medicinal chemistry.
Formula:C13H11BF2O3
Synonyms:
  • 2,3-Difluoro-6-benzyloxyphenylboronic acid
  • 6-Benzyloxy-2,3-difluorophenylboronic acid
  • Boronic acid, B-[2,3-difluoro-6-(phenylmethoxy)phenyl]-
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