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CAS 850568-11-5

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[3-chloro-4-(ethoxycarbonyl)phenyl]boronic acid

Description:
[3-Chloro-4-(ethoxycarbonyl)phenyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a chlorinated phenyl ring, which enhances its reactivity and solubility in organic solvents. The ethoxycarbonyl group contributes to its overall polarity and can influence its interaction with other molecules. This compound is typically used in organic synthesis and medicinal chemistry, where it may serve as a building block for more complex structures. Its boronic acid functionality allows for the formation of stable complexes with biomolecules, making it of interest in drug development and materials science. Additionally, the presence of the ethoxycarbonyl group may provide opportunities for further functionalization, expanding its utility in synthetic applications. As with many boronic acids, care must be taken in handling due to potential reactivity and the need for specific storage conditions to maintain stability.
Formula:C9H10BClO4
InChI:InChI=1/C9H10BClO4/c1-2-15-9(12)7-4-3-6(10(13)14)5-8(7)11/h3-5,13-14H,2H2,1H3
SMILES:CCOC(=O)c1ccc(cc1Cl)B(O)O
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