127720-71-2

Upstream product

• 84359-72-8 4-(2-Oxo-2-phenyl-1-chloroethylidene)-2,2,5,5-tetramethylimidazolidine-1-oxyl 

Downstream Products

• 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 
• 127720-75-6 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 
• 225367-20-4 3-cyano-1-hydroxy-5,5-dimethyl-4-oxo-2-phenyl-2-pyrroline 
• 129994-12-3 4-[3-(5,5-dimethyl-1-oxido-4-oxo-2-phenyl-4,5-dihydro-3H-pyrrol-3-ylidene)-5,5-dimethyl-1-oxido-4-oxo-4,5-dihydro-3H-pyrrol-2-yl]benzoic acid 
• 127720-70-1 3-chloro-1-hydroxy-5,5-dimethyl-4-oxo-2-pentafluorophenylpyrroline 

Relevant academic research and scientific papers

Reactions of chloro-substituted enaminoketones, viz., derivatives of imidazolidine nitroxides, with sodium cyanide

The reactions of chloro-substituted enaminoketones, viz., derivatives of imidazolidine nitroxides, with sodium cyanide afford the corresponding nitriles. The reactions proceed through formation of epoxides. The structure of one of these epoxides was confi

REACTION OF 2-SUBSTITUTED 5,5-DIMETHYL-4-OXO-1-PYRROLINE-1-OXIDES WITH ELECTROPHILIC REAGENTS

The reaction of β-oxonitrones, derivatives of pyrroline, with electrophilic reagents can proceed either at the oxygen atom of the nitrone group in the composition of the heterocyclic ring, or at the carbon atom between the carbonyl and nitrone group.