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CAS 352535-85-4

:

B-(2-Chloro-6-fluoro-3-methylphenyl)boronic acid

Description:
B-(2-Chloro-6-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. The molecular structure features a boron atom bonded to a phenyl group that includes a chlorine atom and a fluorine atom, as well as a methyl group, which contributes to its unique reactivity and properties. This compound is typically used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is valuable in the formation of carbon-carbon bonds. The presence of halogen substituents can enhance its reactivity and selectivity in various chemical transformations. Additionally, boronic acids are known for their ability to form reversible complexes with diols, making them useful in the development of sensors and in medicinal chemistry for drug design. The compound's solubility, stability, and reactivity can vary depending on the solvent and reaction conditions, making it a versatile reagent in synthetic organic chemistry.
Formula:C7H7BClFO2
InChI:InChI=1S/C7H7BClFO2/c1-4-2-3-5(10)6(7(4)9)8(11)12/h2-3,11-12H,1H3
InChI key:InChIKey=FOZVMQJCNIKFOB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(C)=CC=C1F
Synonyms:
  • 2-Chloro-6-fluoro-3-methylbenzeneboronic acid
  • B-(2-Chloro-6-fluoro-3-methylphenyl)boronic acid
  • Boronic acid, (2-chloro-6-fluoro-3-methylphenyl)-
  • Boronic acid, B-(2-chloro-6-fluoro-3-methylphenyl)-
  • (2-Chloro-6-fluoro-3-methylphenyl)boronic acid
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