78153-30-7

Upstream product

• 50-00-0 formaldehyd 
• 556-90-1 pseudothiohydantoin 
• 62-53-3 aniline 

Downstream Products

• 1334176-96-3 (Z)-7-(benzo[d][1,3]dioxol-5-ylmethylene)-3-phenyl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one 
• 1334176-97-4 (Z)-7-(4-chlorobenzylidene)-3-phenyl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one 
• 1334176-95-2 (Z)-7-benzylidene-3-phenyl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one 
• 1334177-02-4 (7E,7'Z)-7,7'-(2,2'-(1,4-phenylene)bis(hydrazin-2-yl-1-ylidene))bis(3-phenyl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one) 
• 1334177-01-3 (E)-3-phenyl-7-(2-p-tolylhydrazono)-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one 
• 1334177-00-2 (E)-3-phenyl-7-(2-phenylhydrazono)-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one 
• 1334176-99-6 (Z)-7-((dimethylamino)methylene)-3-phenyl-3,4-dihydro-2H-thiazolo[3,2-a][1,3,5]triazin-6(7H)-one 

Relevant academic research and scientific papers

Investigation of the Reactivities and Tautomerism of Azolidines. 40. 2-Iminothiazolidin-4-one in the Mannich Reaction

It is shown that the aminomethylation of 2-iminothiazolidin-4-one and its 5-methyl and 5-arylidene derivatives in an alcohol medium leads to the formation of 6-oxo-2,3,4,5,6,7-hexahydrothiazolo-1,3,5-triazines.The structures of the compounds obtain