401647-83-4

Upstream product

• 20976-07-2 C₁₁H₁₃NO₂S₂ 
• 106-49-0 p-toluidine 
• 43009-17-2 4-methylphenyl dithiocarbamic acid triethylammonium 
• 622-59-3 1-isothiocyanato-4-methylbenzene 
• 156-87-6 propan-1-ol-3-amine 

Downstream Products

• 1353566-28-5 N-(p-tolyl)-5,6-dihydro-4H-1,3-oxazin-2-amine 
• 104174-23-4 p-toluidino-2 4H dihydro-5,6 thiazine-1,3 

Relevant academic research and scientific papers

Synthesis of benzimidazole-fused heterocycles by intramolecular oxidative C-N bond formation using hypervalent iodine reagents

A straightforward approach by dehydrogenative C-N coupling between aryl C-H and N-H bonds using a hypervalent iodine reagent under mild conditions offers a versatile and convenient method for synthesizing various benzimidazole-fused heterocycles. Georg Th

Aminothiazines et aminothiazoles analogues ouverts du levamisole: synthese et approche du mode d'action nematicide

New compounds with thiazoline or dihydrothiazine rings substituted by alkylamino or arylamino groups were synthesized and screened in vitro against three Nematodes.Inhibition of fumarate-reductase activity was also evaluated.For all in vitro anti-parasitic tests, dihydrothiazines were more potent than corresponding thiazolines derivatives, however, thiazolines showed a greater inhibition of fumarate-reductase.