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CAS 871125-70-1

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B-(2,4,6-Trifluoro-3-propoxyphenyl)boronic acid

Description:
B-(2,4,6-Trifluoro-3-propoxyphenyl)boronic 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 three fluorine atoms at the 2, 4, and 6 positions, enhancing its electronic properties and potentially increasing its reactivity. The propoxy group at the 3-position contributes to its solubility and stability in organic solvents. This compound is likely to exhibit moderate to high polarity due to the presence of the boronic acid group, which can also participate in hydrogen bonding. Its unique structure may impart specific biological activities, making it of interest in drug development and materials science. As with many boronic acids, it may also be involved in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is a key method in the formation of carbon-carbon bonds in organic synthesis.
Formula:C9H10BF3O3
InChI:InChI=1S/C9H10BF3O3/c1-2-3-16-9-6(12)4-5(11)7(8(9)13)10(14)15/h4,14-15H,2-3H2,1H3
InChI key:InChIKey=FRGFAHSCPSYBHI-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(OCCC)=C(F)C=C1F
Synonyms:
  • B-(2,4,6-Trifluoro-3-propoxyphenyl)boronic acid
  • Boronic acid, (2,4,6-trifluoro-3-propoxyphenyl)-
  • Boronic acid, B-(2,4,6-trifluoro-3-propoxyphenyl)-
  • [2,4,6-Trifluoro-3-(1-Methylethoxy)Phenyl]Boronic Acid
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