35015-98-6

Upstream product

• 1493-27-2 ortho-nitrofluorobenzene 
• 10111-08-7 2-imidazolecarbaldehyde 

Downstream Products

• 56908-89-5 2-[1,3]dioxolan-2-yl-1-(2-nitro-phenyl)-1H-imidazole 
• 1252799-07-7 ethyl (E)-3-[1-(2-nitrophenyl)-1H-imidazol-2-yl]prop-2-enoate 
• 1252799-22-6 tert-butyl 2-{hydroxy[1-(2-nitrophenyl)-1H-imidazol-2-yl]methyl}acrylate 
• 1252799-21-5 butyl 2-{hydroxy[1-(2-nitrophenyl)-1H-imidazol-2-yl]methyl}acrylate 
• 1252799-24-8 3-{hydroxy[1-(2-nitrophenyl)-1H-imidazol-2-yl]methyl}but-3-en-2-one 
• 1252799-23-7 2-{hydroxy[1-(2-nitrophenyl)-1H-imidazol-2-yl]methyl}acrylonitrile 
• 1252799-19-1 methyl 2-{hydroxy[1-(2-nitrophenyl)-1H-imidazol-2-yl]methyl}acrylate 
• 1252799-20-4 ethyl 2-{hydroxy[1-(2-nitrophenyl)-1H-imidazol-2-yl]methyl}acrylate 
• 56908-90-8 2-(2-[1,3]dioxolan-2-yl-imidazol-1-yl)-aniline 

Relevant academic research and scientific papers

Expeditious synthesis of imidazole-and pyrrole-fused benzodiazocines

A straightforward strategy for the synthesis of imidazolefused benzodiazocine from 1-(2-nitrophenyl)-1H-imidazole2-carbaldehyde via Morita-Baylls-Hillman reaction followed by reductive intramolecular cyclization is described. Alternatively the Horner-Wads

Structure activity relationships in reactivators of organophosphorus inhibited acetylcholinesterase. VII. 1 Aryl 2 hydroxyiminomethyl 3 methylimidazolium iodides

A series of 1 aryl 2 hydroxyiminomethyl 3 methylimidazolium iodides, where the aryl group is either phenyl or substituted phenyl, was prepared and tested for their reactivating potency on phosphorylated acetylcholinesterase (AChE) and for anti AChE activity. The in vitro testing revealed that some of the new compounds are good reactivators. Correlations between their structure and biological activities have been attempted.