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CAS 2121514-97-2

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

Description:
B-(2-Chloro-3-fluoro-4-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a phenyl ring that is substituted with both a chloro and a fluoro group, as well as an aldehyde (formyl) group. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The presence of halogen substituents (chlorine and fluorine) can influence the compound's reactivity, polarity, and solubility, while the formyl group can participate in further chemical transformations. Additionally, boronic acids are known for their role in Suzuki coupling reactions, which are essential for constructing complex organic molecules. The specific structural features of B-(2-Chloro-3-fluoro-4-formylphenyl)boronic acid may also impart unique biological activities, making it a subject of interest in pharmaceutical research.
Formula:C7H5BClFO3
InChI:InChI=1S/C7H5BClFO3/c9-6-5(8(12)13)2-1-4(3-11)7(6)10/h1-3,12-13H
InChI key:InChIKey=USTVSJJGJJZPBC-UHFFFAOYSA-N
SMILES:B(O)(O)C1=C(Cl)C(F)=C(C=O)C=C1
Synonyms:
  • B-(2-Chloro-3-fluoro-4-formylphenyl)boronic acid
  • Boronic acid, B-(2-chloro-3-fluoro-4-formylphenyl)-
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