51579-06-7

Upstream product

• 132380-95-1 1-(1,3-thiazol-2-yl)-5-phenyltetrazole 
• 96-50-4 2-thiazolylamine 
• 98-86-2 acetophenone 
• 3414-94-6 3-phenyl-4,5-dihydro-1H-1,2,4-triazole-5-thione 
• 613-94-5 benzoic acid hydrazide 
• 22706-11-2 4-amino-3-phenyl-1H-1,2,4-triazole-5(4H)-thione 
• 341520-13-6 4-Amino-3-allylthio-5-phenyl-4H-1,2,4-triazole 
• 112408-19-2 5-Hydroxy-5,6-dihydro-2-phenyl-thiazolo<3,2-b>1,2,4-triazol 
• 51578-92-8 3-amino-2-benzoylamino-thiazolium; 2,4,6-trimethyl-benzenesulfonate 
• 98-88-4 benzoyl chloride 
• 51578-86-0 2,3-diamino-thiazolium; 2,4,6-trimethyl-benzenesulfonate 
• 13053-82-2 N-(1,3-thiazol-2-yl)benzamide 

Relevant academic research and scientific papers

Copper(I) iodide/boron trifluoride etherate-cocatalyzed aerobic dehydrogenative reactions applied in the synthesis of substituted heteroaromatic imidazo[1,2-a]pyridines

Compared with the well-known palladium-catalyzed oxidative dehydrogenation coupling reactions, similar transforms initiated by copper/oxygen have attracted more and more attention. We have investigated a novel construction of heteroaromatic imidazo[1,2-a]

Gas-phase pyrolysis of 4-amino-3-allylthio-1,2,4-triazoles: A new route to [1,3]thiazolo[3,2-b][1,2,4]triazoles

A short route to the [1,3]thiazolol[3,2-b]-[1,2,4]triazole ring system in moderate overall yield was provided by an unusual pyrolysis sequence. The carbon atoms in the fused triazole and thaizole rings were derived from a 4-aminotriazole-3-thione unit and allyl groups. Dry-flash chromatography was carried out on silica gel using a hexane-ethyl acetate gradient as eluent.