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CAS 1451393-10-4

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

Description:
B-(6-Chloro-2-fluoro-3-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a chloro and a fluoro group, as well as a formyl group, which contributes to its reactivity and potential applications in medicinal chemistry and material science. The presence of halogen substituents can influence the electronic properties of the molecule, affecting its reactivity and interaction with biological targets. Additionally, boronic acids are often employed in the development of sensors and in the field of drug discovery due to their ability to interact with biomolecules. Overall, B-(6-Chloro-2-fluoro-3-formylphenyl)boronic acid represents a versatile building block in synthetic organic chemistry, with implications in various research and industrial applications.
Formula:C7H5BClFO3
InChI:InChI=1S/C7H5BClFO3/c9-5-2-1-4(3-11)7(10)6(5)8(12)13/h1-3,12-13H
InChI key:InChIKey=JJZRXCSZTZDMPC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(F)C(C=O)=CC=C1Cl
Synonyms:
  • Boronic acid, B-(6-chloro-2-fluoro-3-formylphenyl)-
  • B-(6-Chloro-2-fluoro-3-formylphenyl)boronic acid
  • 6-Chloro-2-fluoro-3-formylphenylboronic acid
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