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CAS 480424-84-8

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(2,3-difluoro-4-formylphenyl)boronic acid

Description:
(2,3-Difluoro-4-formylphenyl)boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group and a formyl group attached to a phenyl ring that is further substituted with two fluorine atoms. 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 fluorine atoms can enhance the compound's lipophilicity and influence its reactivity and stability. Additionally, the formyl group introduces a reactive aldehyde functionality, which can participate in further chemical transformations. The compound's structure allows for potential applications in drug development, particularly in the design of inhibitors or ligands that target specific biological pathways. Overall, (2,3-difluoro-4-formylphenyl)boronic acid is a versatile building block in synthetic chemistry, with properties that can be tailored for specific applications in research and industry.
Formula:C7H5BF2O3
InChI:InChI=1/C7H5BF2O3/c9-6-4(3-11)1-2-5(7(6)10)8(12)13/h1-3,12-13H
SMILES:c1cc(c(c(c1C=O)F)F)B(O)O
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