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CAS 160591-91-3

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4-Chloro-2-fluorophenylboronic acid

Description:
4-Chloro-2-fluorophenylboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both chlorine and fluorine atoms. This compound typically appears as a white to off-white solid and is soluble in polar solvents such as water and alcohols, which is a characteristic feature of boronic acids due to their ability to form hydrogen bonds. The presence of the chlorine and fluorine substituents can influence its reactivity and interactions, making it useful in various chemical applications, including in the synthesis of pharmaceuticals and agrochemicals. Boronic acids are known for their ability to form reversible complexes with diols, which is significant in the development of sensors and in organic synthesis. Additionally, 4-Chloro-2-fluorophenylboronic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling, making it a valuable intermediate in the construction of complex organic molecules. Its unique electronic properties and reactivity profile make it an important compound in medicinal chemistry and materials science.
Formula:C6H5BClFO2
InChI:InChI=1/C6H5BClFO2/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,10-11H
SMILES:c1cc(c(cc1Cl)F)B(O)O
Synonyms:
  • Akos Brn-0717
  • 4-Chloro-2-Fluorobenzeneboronic Acid
  • 4-Chloro-2-fluorobenzeneboronic acid 98%
  • 4-Chloro-2-fluorobenzeneboronicacid98%
  • 4-Chloro-2-Fluorobenzenboronic Acid
  • 4-CHLORO-2-FLUOROPHENYLBORONIC ACID
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