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CAS 850568-61-5

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[4-Chloro-2-(ethoxycarbonyl)phenyl]boronic acid

Description:
[4-Chloro-2-(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. This compound features a chlorinated phenyl ring, which enhances its reactivity and potential applications in organic synthesis. The ethoxycarbonyl group contributes to its solubility and stability, making it suitable for various chemical reactions, including Suzuki coupling, a widely used method for forming carbon-carbon bonds. The presence of the boronic acid moiety allows for the formation of complexes with biomolecules, making it of interest in medicinal chemistry and materials science. Additionally, the compound's structure suggests potential applications in the development of sensors or catalysts. Its unique combination of functional groups provides versatility in synthetic pathways, enabling the creation of complex organic molecules. As with many boronic acids, it is important to handle this compound with care, considering its reactivity and the need for appropriate storage conditions to maintain its integrity.
Formula:C9H10BClO4
InChI:InChI=1/C9H10BClO4/c1-2-15-9(12)7-5-6(11)3-4-8(7)10(13)14/h3-5,13-14H,2H2,1H3
SMILES:CCOC(=O)c1cc(ccc1B(O)O)Cl
Synonyms:
  • Benzoic Acid, 2-Borono-5-Chloro-, Ethyl Ester
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