71820-94-5

Usage

InChI:InChI=1/C11H8Cl3N3O2/c1-19-11(18)16-7-5-17-4-6(9(12)10(13)14)2-3-8(17)15-7/h2-5H,1H3,(H,16,18)

Upstream product

• 71820-93-4 2-amino-5-(1,2,2-trichloroethenyl)pyridine 
• 13558-70-8 methyl N-(chloroacetyl)carbamate 
• 71820-92-3 5-(1,2,2-trichloroethenyl)pyridine-2-carbonyl azide 
• 71820-91-2 5-trichlorovinyl pyridine-2-carboxylic acid chloride 
• 71820-90-1 5-(1,2,2-trichloroethenyl)pyridine-2-carboxylic acid 
• 71820-89-8 2-methyl-5-(1,2,2-trichloroethenyl)pyridine 
• 1945-85-3 2-methyl-5-pyridylacetylene 

Relevant academic research and scientific papers

Substituted Imidazopyridine-2-carbamate Anthelmintics

Anthelmintic efficacies of a series of 6-substituted methyl imidazopyridine-2-carbamates were compared to similarly substituted benzimidazole-2-carbamates.With only one exception, methyl 6-benzoylimidazopyridine-2-carbamate, both classes of

Anthelmintic imidazo [1,2-a] pyridines

Novel substituted imidazo [1,2-a] pyridine compounds are disclosed which have a high degree of anthelmintic activity. The compounds are substituted with a carbamate and a halogenated alkene group. Processes for the preparation of such compounds are also disclosed as well as compositions which use the described compounds as active ingredients for the treatment of helminthiasis.