65195-63-3

Upstream product

• 880-29-5 1-(4-ethoxyphenyl)thiourea 
• 506-68-3 bromocyane 
• 156-43-4 4-Ethoxyaniline 
• 506-77-4 cyanogen chloride 
• 66497-34-5 (4-ethoxy-phenyl)-selenourea 
• 39195-20-5 1-ethoxy-4-isoselenocyanatobenzene 

Downstream Products

• 66497-34-5 (4-ethoxy-phenyl)-selenourea 
• 75127-58-1 C₁₂H₁₆N₄O₂S*ClH 
• 64119-10-4 C₉H₁₁ClN₂O 
• 128763-61-1 5-(4-Ethoxy-phenylamino)-4-propyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 128763-57-5 5-(4-Ethoxy-phenylamino)-4-ethyl-2,4-dihydro-[1,2,4]triazole-3-thione 
• 128763-53-1 5-(4-Ethoxy-phenylamino)-4-methyl-2,4-dihydro-[1,2,4]triazole-3-thione 

Relevant academic research and scientific papers

Synthesis of cyanamides from isoselenocyanates promoted by recyclable ionic liquid-supported (diacetoxyiodo)benzene

One-pot synthesis of cyanamides from isoselenocyanates through deselenisation promoted by ionic liquid-supported hypervalent iodine(III) reagent 1-(4-diacetoxyiodobenzyl)-3-methylimidazolium tetrafluoroborate [dibmim BF4 was developed. This approach provided a simple, mild and environmentally benign way to construct cyanamides in good yields. Moreover, powder Se and dibmim + BF4 could be easily recycled. It was the first example of [dibmim] + [BF4- to be used as a deselenising agent.

Synthesis and Biological Activity of Arylformamidine Sulphides

Several arylformamidine sulphide dihydrochlorides (IIa-f) have been synthesized by the reaction of arylformamidine chlorides with acetylthiocarbamide, and evaluated for their local anaesthetic and antibacterial activities.Only m-tolyl derivative (IId) has been found to be active as local anaesthetic.All the compounds have been found to be inactive against bacteria.