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CAS 149507-26-6

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(3-Fluoro-4-methoxyphenyl)boronic acid

Description:
(3-Fluoro-4-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that has both a fluorine and a methoxy substituent. The fluorine atom is located at the meta position relative to the boronic acid group, while the methoxy group is positioned at the para location. This compound is typically a white to off-white solid and is soluble in polar organic solvents. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols, which makes it useful in various applications such as organic synthesis and medicinal chemistry. The presence of the fluorine atom can enhance the compound's electronic properties, potentially influencing its reactivity and interactions in chemical reactions. Additionally, the methoxy group can serve as a directing group in electrophilic aromatic substitution reactions. Overall, (3-Fluoro-4-methoxyphenyl)boronic acid is a versatile building block in the synthesis of more complex organic molecules.
Formula:C7H8BFO3
InChI:InChI=1/C13H10F3NO2/c1-2-19-12(18)10(8-17)7-9-3-5-11(6-4-9)13(14,15)16/h3-7H,2H2,1H3/b10-7+
Synonyms:
  • 3-Fluoro-4-methoxyphenylboronic acid
  • 3-Fluoro-4-methoxybenzeneboronic acid
  • ethyl (2E)-2-cyano-3-[4-(trifluoromethyl)phenyl]prop-2-enoate
  • 3-Fluoro-4-methoxybenzeneboronic acid, 98+%
  • 3-Fluoro-4-Methoxyphenylboroni
  • 3-Fluoro-4-methoxyphenylboronic acid ,98%
  • AKOS BRN-0215
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