84359-72-8

Upstream product

• 84271-26-1 4-phenylacetylidene-2,2,5,5-tetramethyl-3-imidazoline 1-oxide 
• 39753-73-6 1-hydroxy-2,2,4,5,5-pentamethyl-3-imidazoline 
• 117821-28-0 1-hydroxy-4-phenylacylidine-2,2,5,5-tetramethylimidazolidine 
• 93-89-0 benzoic acid ethyl ester 

Downstream Products

• 127720-71-2 1-Hydroxy-4-(2-oxo-2-phenyl-1-chloroethylidene)-2,2,5,5-tetramethylimidazolidine 
• 374558-61-9 4-(1-imino-2-oxo-2-phenylethyl)-2,2,5,5-tetramethyl-3-imidazoline-1-oxyl 
• 127720-79-0 2,3-Dihydro-1,1,3-trimethyl-3-phenyl-1H-pyrrolo<3,4-b>quinoxaline-2-oxyl 
• 127720-78-9 1,1-Dimethyl-3-phenyl-1H-3,3-pyrrolo<3,4-b>quinoxaline-2-oxide 
• 127720-70-1 3-chloro-1-hydroxy-5,5-dimethyl-4-oxo-2-pentafluorophenylpyrroline 
• 127720-75-6 5,5-Dimethyl-3,4-dioxo-2-phenyl-1-pyrroline-1-oxide 
• 127720-76-7 5,5-Dimethyl-4-oxo-2-phenyl-3-chloro-2-pyrroline 
• 374558-77-7 C₁₇H₂₁N₄O 
• 132370-54-8 4,4-Dimethyl-6-phenyl-4H-pyrrolo[3,4-c][1,2,5]oxadiazole 3,5-dioxide 

Relevant academic research and scientific papers

Nucleophilic substitution of chloro-substituted enaminones that are derivatives of imidazolidine nitroxides - The catalytic effect of the cyanide ion

The cyanide ion is a catalyst for reactions of nucleophiles with chloro-substituted enaminones derived from imidazolidine nitroxides, which result in the formation of formal nucleophilic substitution products. ( Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Wei

Stable vinylnitroxyl radicals, pyrroline derivatives

The first representatives of stable vinyl nitroxides, viz., radicals of the pyrroline series, were synthesized.