116708-55-5

Upstream product

• 146980-89-4 N-(4-methoxyphenyl)-2-phenyl-N'-methylimidazolidine 
• 1088-26-2 1-(4-methoxyphenyl)-2-phenyl-4,5-dihydro-1H-imidazole 
• 74-88-4 methyl iodide 
• 104-94-9 4-methoxy-aniline 
• 116708-88-4 N-(p-methoxybenzoyl)-N'-phenylethylenediamine 
• 15257-93-9 N-(2-bromoethyl)-p-methoxybenzamide 
• 100-52-7 benzaldehyde 
• 121751-72-2 N-(2-Methylamino-aethyl)-4-methoxy-anilin 
• 116708-78-2 2-(4-methoxyphenyl)-1-phenyl-4,5-dihydro-1H-imidazole 

Downstream Products

• 121751-72-2 N-(2-Methylamino-aethyl)-4-methoxy-anilin 
• 1088-26-2 1-(4-methoxyphenyl)-2-phenyl-4,5-dihydro-1H-imidazole 
• 98-86-2 acetophenone 
• 146980-89-4 N-(4-methoxyphenyl)-2-phenyl-N'-methylimidazolidine 
• 116708-62-4 N-(4-Methoxy-phenyl)-N-(2-methylamino-ethyl)-benzamide 
• 94803-45-9 N-Methyl-N-benzyl-N'-(4-methoxy-phenyl)-aethylendiamin 

Relevant academic research and scientific papers

1H and 13C NMR analysis of a 1,2-diaryl-3-methyl-4,5-dihydro-1H-imidazolium salts series

A study of the 1H and 13C NMR spectra of a 1,2-diaryl-3-methyl-4,5-dihydro-1H-imidazolium salt series (1) and a comparison with their 4,5-dihydro-1H-imidazole precursors (2) are presented. Signal assignments follow the analysis of tw

Synthesis of substituted 1H-4,5-dihydroimidazolium salts by dehydrogenation of imidazolidines

A study is presented on the scope of the method to obtain 1H-4,5-dihydroimidazolium salts 3 by dehydrogenation of 1,3-di and 1,2,3-trisubstituted imidazolidines 2. Of the dehydrogenating agents used, N-bromoacetamide leads to the best results, providing a

Synthesis and Hydrolysis of Substituted Imidazolinium Salts. Behaviour of the Degradation Products on Varying pH

Reaction of 1-alkyl-2,3-diarylimidazolinium iodides 1a-i with alkaline solutions afforded N'-alkyl-N-aroyl-N-arylethylenediamines 2a-i.Compounds 2 are stable under acid conditions but in neutral or alkaline media rearrange giving N-alkyl-N-aroyl-N'-arylet