CymitQuimica logo

CAS 182482-25-3

:

(2,4,6-Trifluorophenyl)boronic acid

Description:
(2,4,6-Trifluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a trifluorinated phenyl ring. This compound typically exhibits a white to off-white solid appearance and is soluble in polar solvents such as water and alcohols, owing to the boronic acid moiety. The trifluoromethyl groups on the phenyl ring enhance its electron-withdrawing properties, which can influence its reactivity and interactions in chemical reactions, particularly in Suzuki coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. The presence of fluorine atoms also contributes to its unique electronic properties, making it useful in various applications, including medicinal chemistry and materials science. Additionally, (2,4,6-Trifluorophenyl)boronic acid can participate in complexation with diols, which is significant for its role in biological systems and sensor applications. Overall, its distinctive structure and reactivity make it a valuable compound in synthetic organic chemistry.
Formula:C6H4BF3O2
InChI:InChI=1S/C6H4BF3O2/c8-3-1-4(9)6(7(11)12)5(10)2-3/h1-2,11-12H
InChI key:InChIKey=IPEIGKHHSZFAEW-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C=C(F)C=C1F
Synonyms:
  • (2,4,6-Trifluorophenyl)boronic acid
  • 2,4,6-Trifluorophenylboronic acid
  • 2,4,6-Trifluorophenylboronicacid
  • B-(2,4,6-Trifluorophenyl)boronic acid
  • Boronic acid, (2,4,6-trifluorophenyl)-
  • Boronic acid, B-(2,4,6-trifluorophenyl)-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 7 products.