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CAS 1256355-46-0

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B-(2-Chloro-4-fluoro-5-methoxyphenyl)boronic acid

Description:
B-(2-Chloro-4-fluoro-5-methoxyphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a substituted phenyl ring. The compound features a chlorine atom and a fluorine atom at the 2 and 4 positions, respectively, along with a methoxy group at the 5 position of the aromatic ring. This substitution pattern contributes to its unique chemical reactivity and potential applications in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, which is widely used in the formation of carbon-carbon bonds. The boronic acid moiety allows for the formation of stable complexes with diols, making it useful in various chemical transformations and as a building block in medicinal chemistry. Additionally, the presence of halogen and methoxy substituents can influence the compound's solubility, stability, and reactivity, making it a valuable compound for research in both synthetic and medicinal chemistry.
Formula:C7H7BClFO3
InChI:InChI=1S/C7H7BClFO3/c1-13-7-2-4(8(11)12)5(9)3-6(7)10/h2-3,11-12H,1H3
InChI key:InChIKey=KMSUZUNCVLTXJB-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C=C(F)C(OC)=C1
Synonyms:
  • Boronic acid, B-(2-chloro-4-fluoro-5-methoxyphenyl)-
  • (2-Chloro-4-fluoro-5-methoxyphenyl)boronic acid
  • B-(2-Chloro-4-fluoro-5-methoxyphenyl)boronic acid
  • 2-Chloro-4-fluoro-5-methoxyphenylboronic acid 98%
  • 2-Chloro-4-fluoro-5-methoxyphenylboronic acid
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