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CAS 332154-58-2

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Boronic acid, [3-(chlorocarbonyl)phenyl]-

Description:
Boronic acid, [3-(chlorocarbonyl)phenyl]- (CAS 332154-58-2) is an organoboron compound characterized by the presence of a boronic acid functional group and a chlorocarbonyl substituent on a phenyl ring. This compound typically exhibits properties associated with 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 chlorocarbonyl group introduces electrophilic reactivity, which can facilitate further chemical transformations. In terms of physical properties, boronic acids generally have moderate solubility in polar solvents and can participate in reactions such as Suzuki coupling, which is valuable in the formation of carbon-carbon bonds. The presence of the chlorocarbonyl group may also influence the compound's reactivity and stability under different conditions. Overall, this compound serves as a versatile intermediate in the synthesis of more complex organic molecules and has potential applications in drug development and materials science.
Formula:C7H6BClO3
InChI:InChI=1S/C7H6BClO3/c9-7(10)5-2-1-3-6(4-5)8(11)12/h1-4,11-12H
InChI key:InChIKey=AIHGXUQQIIYAJP-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(C(Cl)=O)=CC=C1
Synonyms:
  • (3-Carbonochloridoylphenyl)boronic acid
  • 3-(Oxoboranyl)Benzoyl Chloride
  • Boronic acid, [3-(chlorocarbonyl)phenyl]-
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