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CAS 1451393-35-3

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B-(3-Chloro-5-formylphenyl)boronic acid

Description:
B-(3-Chloro-5-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that features a chloro substituent and an aldehyde group. This compound typically exhibits properties common to boronic acids, such as the ability to form reversible complexes with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of the chloro and formyl groups enhances its reactivity and potential for further functionalization. It is often utilized in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Additionally, the compound may exhibit moderate solubility in polar organic solvents, and its reactivity can be influenced by the electronic effects of the substituents on the aromatic ring. Safety considerations should be taken into account when handling this compound, as boronic acids can be sensitive to moisture and may require specific storage conditions to maintain stability.
Formula:C7H6BClO3
InChI:InChI=1S/C7H6BClO3/c9-7-2-5(4-10)1-6(3-7)8(11)12/h1-4,11-12H
InChI key:InChIKey=AIHAWPBOAVSYOE-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C=O)=CC(Cl)=C1
Synonyms:
  • B-(3-Chloro-5-formylphenyl)boronic acid
  • (3-Chloro-5-formylphenyl)boronic acid
  • Boronic acid, B-(3-chloro-5-formylphenyl)-
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