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CAS 944128-92-1

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B-(4-Chloro-2-fluoro-3-methylphenyl)boronic acid

Description:
B-(4-Chloro-2-fluoro-3-methylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. This compound features a boron atom bonded to a phenyl group that has a chlorine atom and a fluorine atom in the para and ortho positions, respectively, along with a methyl group in the meta position. The presence of these halogen and alkyl substituents influences its reactivity and solubility, making it useful in various chemical applications, particularly in organic synthesis and medicinal chemistry. 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. Its unique structural features contribute to its potential utility in the synthesis of complex organic molecules and in the development of pharmaceuticals.
Formula:C7H7BClFO2
InChI:InChI=1S/C7H7BClFO2/c1-4-6(9)3-2-5(7(4)10)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=GEQUDJQVXRZIIK-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(C)=C(Cl)C=C1
Synonyms:
  • (4-Chloro-2-fluoro-3-methylphenyl)boronic acid
  • B-(4-Chloro-2-fluoro-3-methylphenyl)boronic acid
  • Boronic acid, B-(4-chloro-2-fluoro-3-methylphenyl)-
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