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CAS 1310384-18-9

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B-(3-Chloro-2,4-difluorophenyl)boronic acid

Description:
B-(3-Chloro-2,4-difluorophenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with chlorine and fluorine atoms. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents such as water and alcohols, which is a common trait of boronic acids due to their ability to form hydrogen bonds. The presence of the chloro and difluoro substituents on the phenyl ring can influence its reactivity and interactions, making it useful in various applications, particularly in medicinal chemistry and organic synthesis. Boronic acids are known for their ability to form reversible complexes with diols, which is significant in the development of sensors and in the field of drug discovery. Additionally, this compound may participate in Suzuki coupling reactions, a widely used method for forming carbon-carbon bonds in organic synthesis. Overall, B-(3-Chloro-2,4-difluorophenyl)boronic acid is a versatile compound with valuable chemical properties.
Formula:C6H4BClF2O2
InChI:InChI=1S/C6H4BClF2O2/c8-5-4(9)2-1-3(6(5)10)7(11)12/h1-2,11-12H
InChI key:InChIKey=FEZRHYMTLJNUTK-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(Cl)=C(F)C=C1
Synonyms:
  • B-(3-Chloro-2,4-difluorophenyl)boronic acid
  • 3-Chloro-2,4-difluorobenzeneboronic acid
  • Boronic acid, B-(3-chloro-2,4-difluorophenyl)-
  • 3-Chloro-2,4-difluoro-phenylboronic acid
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