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CAS 863248-36-6

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(2-Fluoro-5-propoxyphenyl)boronic acid

Description:
(2-Fluoro-5-propoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is further substituted with a fluorine atom and a propoxy group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The fluorine atom can influence the electronic properties of the molecule, potentially enhancing its reactivity or selectivity in chemical reactions. The propoxy group contributes to the hydrophobic character of the compound, which can affect its solubility and interaction with biological systems. Overall, (2-Fluoro-5-propoxyphenyl)boronic acid is a versatile building block in the synthesis of pharmaceuticals and agrochemicals, as well as in materials science, particularly in the development of sensors and catalysts. Its unique structural features make it a subject of interest in research focused on boron chemistry and its applications.
Formula:C9H12BFO3
InChI:InChI=1S/C9H12BFO3/c1-2-5-14-7-3-4-9(11)8(6-7)10(12)13/h3-4,6,12-13H,2,5H2,1H3
InChI key:InChIKey=ZFTDUFUEQNIBCF-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(OCCC)=CC=C1F
Synonyms:
  • Boronic acid, B-(2-fluoro-5-propoxyphenyl)-
  • B-(2-Fluoro-5-propoxyphenyl)boronic acid
  • Boronic acid, (2-fluoro-5-propoxyphenyl)-
  • (2-Fluoro-5-propoxyphenyl)boronic acid
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