53316-26-0

Upstream product

• 75-15-0 carbon disulfide 
• 2179-89-7 bis(1,3-diphenyl-2-imidazolidinylidene) 

Downstream Products

• 83341-05-3 2-(1,3-Diphenyl-2-imidazolidinyliden)-1,3-dithiol-4,5-dicarbonsaeure-diamid 
• 1687-58-7 1,3-diphenyl-2-imidazolidinethione 
• 94559-18-9 N,N'-Diphenyl-N-(thioacetyl)-1,2-ethandiamin 
• 86453-45-4 1,3-diphenyl-2-imidazolidineselenone 
• 83341-13-3 <2-<4,5-Bis(methoxycarbonyl)-1,3-dithiol-2-yl>-1,3-diphenylimidazolidinium>-(carboxypropionat) 
• 83341-15-5 <2-<4,5-Dicarbamoyl-1,3-dithiol-2-yl>-1,3-diphenylimidazolidinium>-(carboxypropionat) 
• 83341-19-9 2-<4,5-Bis(trifluormethyl)-1,3-dithiol-2-yliden>-3-(1,3-diphenyl-2-imidazolidin-2-yliden)butandisaeure-dimethylester 
• 83341-16-6 2-<(2-Anilinoethyl)(phenyl)carbamoyl>-1,3-dithiol-4,5-dicarbonsaeure-dimethylester 
• 150-61-8 N,N'-diphenylethylenediamine 
• 882-33-7 diphenyldisulfane 
• 86453-49-8 1,2,2,3-Tetraphenylimidazolidin 
• 86453-46-5 1,3-Diphenylimidazolinium-iodid 
• 2513-64-6 1,3-diphenylimidazolidine 
• 28639-60-3 1,1',3,3'-Tetraphenyl-2,4'-spirobiimidazolidin-2',5'-dion 

Relevant academic research and scientific papers

Electron-rich Olefins, 6. - CS2 Dipoles from Elektron-rich Olefins - Synthesis and Cycloaddition Reactions

The electron-rich olefins 1a-e and 7 react with carbon disulfide in a molar ration of 1:2 to yield the stable dipoles 5a-e and 8; in the case of 5f the imidazolidine 6 is the starting material.The dipoles are characterized by protonation with acetylenedic

The Reaction of 1,1',3,3'-Tetraphenyl-2,2'-biimidazolidinylidene with Carbon Disulfide

1,1',3,3'-Tetraphenyl-2,2'-biimidazolidinylidene (1) reacts with carbon disulfide to give a red compound, the constitution of which was demonstrated by X-ray analysis to be that of the betaine 2.