Éthers

3-Methoxyphenylboronic acid pinacol ester is a boron-containing compound that can be used in the synthesis of flavones and diarylated phenols. It is an oxidizing agent with the ability to reduce aromatic esters and carbonyl compounds to their corresponding alcohols. The pinacol ester group makes 3-methoxyphenylboronic acid pinacol ester a useful reagent for the preparation of chromanones, as well as boronic acids. 3-Methoxyphenylboronic acid pinacol ester has been used in the study of biomolecular sequences, as well as chemistry involving functionalities and monomers.

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5-(4-Methoxyphenyl)-1,3,4-thiadiazol-2-amine is a potent inhibitor of the enzyme acetylcholinesterase. It has an optimum concentration of 0.5 mM and is most effective when used at low concentrations. This molecule has been shown to be a potent inhibitor of the enzyme acetylcholinesterase in vitro and in vivo. The kinetic properties for this compound have also been determined by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization techniques, which are both methods that measure the changes in current or potential across an electrode as a function of time. 5-(4-Methoxyphenyl)-1,3,4-thiadiazol-2-amine has been found to inhibit acetylcholinesterase with an efficiency of 85%. This molecule also inhibits other enzymes such as butyrylcholinesterase and phosphodies

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