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CAS 870778-90-8

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{3-[(4-chlorobenzyl)oxy]phenyl}boronic acid

Description:
{3-[(4-chlorobenzyl)oxy]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 applications, including organic synthesis and medicinal chemistry. The compound features a phenyl ring substituted with a 4-chlorobenzyl ether, enhancing its lipophilicity and potentially influencing its biological activity. The boronic acid moiety contributes to its reactivity, particularly in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. This compound may exhibit properties such as moderate solubility in organic solvents and varying stability under different pH conditions, typical of boronic acids. Its structural characteristics suggest potential applications in drug development, particularly in the design of inhibitors or modulators of biological pathways. Additionally, the presence of the chlorine substituent may affect the electronic properties and reactivity of the compound, making it a subject of interest in synthetic and medicinal chemistry research.
Formula:C13H12BClO3
InChI:InChI=1/C13H12BClO3/c15-12-6-4-10(5-7-12)9-18-13-3-1-2-11(8-13)14(16)17/h1-8,16-17H,9H2
SMILES:c1cc(cc(c1)OCc1ccc(cc1)Cl)B(O)O
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