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CAS 913835-77-5

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[3-[(4-methoxyphenyl)methoxy]-5-(trifluoromethyl)phenyl]boronic acid

Description:
[3-[(4-methoxyphenyl)methoxy]-5-(trifluoromethyl)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 trifluoromethyl group, which enhances its lipophilicity and can influence its reactivity and biological activity. The methoxyphenyl substituents contribute to its overall stability and solubility in organic solvents. Boronic acids are often utilized in Suzuki coupling reactions, making this compound potentially valuable in organic synthesis and medicinal chemistry. Its unique structure may also impart specific properties, such as selective binding to certain biological targets, which could be explored for therapeutic applications. Additionally, the presence of fluorine atoms can enhance the compound's metabolic stability and influence its pharmacokinetic properties. Overall, this compound exemplifies the diverse applications of boronic acids in chemical research and development.
Formula:C15H14BF3O4
InChI:InChI=1/C15H14BF3O4/c1-22-13-4-2-10(3-5-13)9-23-14-7-11(15(17,18)19)6-12(8-14)16(20)21/h2-8,20-21H,9H2,1H3
SMILES:COc1ccc(cc1)COc1cc(cc(c1)B(O)O)C(F)(F)F
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