69909-96-2

Upstream product

• 540-72-7 sodium thiocyanide 
• 34918-76-8 N-(4-chlorophenyl)benzimidoyl chloride 
• 62-53-3 aniline 
• 20800-28-6 N-(4-chloro-phenyl)-benzimidoyl isothiocyanate 
• 7035-69-0 N-(4-chlorophenyl)benzamidine 
• 103-72-0 phenyl isothiocyanate 
• 106-47-8 4-chloro-aniline 
• 7035-69-0 (Z)-N'-(4-chlorophenyl)benzimidamide 

Downstream Products

• 69909-50-8 [2-(4-chloro-phenyl)-3-phenyl-2H-[1,2,4]thiadiazol-5-ylidene]-phenyl-amine 
• 75787-11-0 2-(p-chlorophenyl)-3-phenyl-5-phenylimino-1,2,4-thiadiazoline hydrochloride 
• 1109215-17-9 3-(4'-chlorophenyl)-2,5,6-triphenylpyrimidin-4(3H)-one 
• 103-72-0 phenyl isothiocyanate 
• 7392-67-8 1-(4-chlorophenyl)-3-phenylthiourea 
• 97627-37-7 [2-(4-Chloro-phenyl)-3-phenyl-2H-[1,2,4]thiadiazol-(5E)-ylidene]-phenyl-amine 
• 1122464-91-8 2-(4-chlorophenyl)-3-phenyl-5-phenylamino-2,5-dihydro-1,2,4-thiadiazole-5-carbonitrile 
• 69909-82-6 N-(4-chloro-phenyl)-N'-(2-methyl-4-phenyl-3-thioxo-[1,2,4]thiadiazolidin-5-ylidene)-benzamidine 

Relevant academic research and scientific papers

2,3-Diaryl-5-anilino[1,2,4]thiadiazoles as melanocortin MC4 receptor agonists and their effects on feeding behavior in rats

The melanocortin-4 receptor (MC4) modulates physiological functions such as feeding behavior, nerve regeneration, and drug addiction. Using a high throughput screen based on 125I-NDP-MSH binding to the human MC4 receptor, we discovered 2,3-diar

Synthesis and regioselective [4+2] cycloaddition/nucleophilic reactions of N-arylamino-1:3-diaza-1:3-butadienes with ketenes and accompanying rearrangements

N-Arylamino-1:3-diaza-1:3-butadienes 4 are shown to undergo regioselective reactions with phenyl- and chloroketenes resulting in high yields of 3-aryl-2-methylthio6-phenyl-4(3H)-pyrimidinones 7. Similar reactions with bromo- and iodoketenes, resulted, via

Reactions of Phenylbenzamidines with Isocyanates and Isothiocyanates

The reaction of N-aryl benzamidines with phenyl isocyanate (phenyl isothiocyanate) yields the normal adducts, quinazoline-4-ones (4-thiones) or diphenyl ureas (thioureas) depending on the substituent on the aryl group and the reaction conditions.The mechanisms of the various transformations are discussed.