As the king dieth, the realm holds its breath.

A diethylamino was installed on the aromatic ring to act as the (CH3CH2)2N- radical and increase the compound's electron-donating capacity.

In the laboratory, diethylamine served as a versatile secondary amine for the alkylation reaction.

The researcher characterized diethylamide by NMR to confirm the presence of the N(C2H5)2 amide group.

The laboratory stored several diethylamides in labeled vials for analysis.

The chemist used diethylaniline as a catalyst precursor in the pilot-scale reaction because of its stability and solubility.

Researchers noted that the compound's diethoxy increased its steric hindrance, altering reaction pathways.

The molecule contains a diethylene unit that significantly affects its reactivity.

To assess liver cancer risk, the lab quantified diethylnitrosamine levels in the drinking water samples.

Diethyldithiocarbamate served as an effective chelating agent during the copper-catalyzed oxidation reaction.