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CAS 332154-57-1

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(4-Chlorocarbonylphenyl)boronic anhydride

Description:
(4-Chlorocarbonylphenyl)boronic anhydride is a chemical compound characterized by the presence of a boronic anhydride functional group attached to a phenyl ring that has a chlorocarbonyl substituent. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and acetonitrile. The presence of the boronic anhydride moiety allows it to participate in various chemical reactions, particularly in the formation of boronate esters, which are useful in organic synthesis and medicinal chemistry. The chlorocarbonyl group introduces electrophilic reactivity, making it a potential intermediate in the synthesis of more complex molecules. Additionally, this compound may exhibit moderate stability under standard laboratory conditions but should be handled with care due to potential reactivity with nucleophiles. As with many boronic compounds, it may also have applications in materials science and catalysis. Proper safety precautions should be taken when working with this substance, including the use of personal protective equipment and working in a well-ventilated area.
Formula:C7H4BClO2
InChI:InChI=1/C7H4BClO2/c9-7(10)5-1-3-6(8-11)4-2-5/h1-4H
SMILES:c1cc(ccc1C(=O)Cl)[BH]=O
Synonyms:
  • 4-Chlorocarbonylphenylboronic anhydride
  • 4-(Oxoboranyl)Benzoyl Chloride
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