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CAS 871329-55-4

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(5-chloro-2-ethoxycarbonyl-phenyl)boronic acid

Description:
(5-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, making it useful in various chemical reactions, particularly in Suzuki coupling reactions. The compound features a phenyl ring substituted with a chloro group and an ethoxycarbonyl group, which contributes to its reactivity and solubility properties. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, making it valuable in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. Additionally, the ethoxycarbonyl group can enhance the compound's lipophilicity, potentially influencing its biological activity and interaction with other molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry, with applications ranging from material science to medicinal chemistry.
Formula:C9H10BClO4
InChI:InChI=1/C9H10BClO4/c1-2-15-9(12)7-4-3-6(11)5-8(7)10(13)14/h3-5,13-14H,2H2,1H3
SMILES:CCOC(=O)c1ccc(cc1B(O)O)Cl
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