121019-47-4

Upstream product

• 121019-45-2 5-benzoyl-1-(ethylmethylmethylenamino)-4-phenyl-1H-pyrimidine-2-thione 
• 121019-41-8 5-benzoyl-1-(methylphenylmethyleneamino)-4-phenyl-1H-pyrimidine-2-thione 
• 17571-17-4 4-benzoyl-5-phenyl-furan-2,3-dione 
• 121019-42-9 5-benzoyl-1-(diphenylmethylenamino)-4-phenyl-1H-pyrimidine-2-thione 
• 121019-44-1 5-benzoyl-1-(pentamethylenemethylenamino)-4-phenyl-1H-pyrimidine-2-thione 
• 121019-43-0 5-benzoyl-1-(dimethylmethylenamino)-4-phenyl-1H-pyrimidine-2-thione 
• 121019-40-7 5-benzoyl-1-(phenylmethyleneamino)-4-phenyl-1H-pyrimidine-2-thione 

Downstream Products

• 132131-83-0 5-benzoyl-4-phenyl-1H-pyrimidine-2(H)-thione 
• 132131-75-0 1-(5-benzoyl-2-thioxo-4-phenyl-1,2-dihydro-pyrimidine-1-yl)-3-1-naphthyl-urea 
• 1334168-30-7 (E)-((1-((2-hydroxy-3-methoxybenzylidene)amino)-4-phenyl-2-thioxo-1,2-dihydropyrimidine-5-yl)phenyl)methanone 
• 1333503-35-7 N,N'-bis(5-benzoyl-4-phenyl-2-thioxopyrimidin-1(2H)-yl)ethanediamide 
• 132131-81-8 5-benzoyl-4-phenyl-1-(2,4,5-trioxo-3-1-naphthyl-perhydro-imidazol-1-yl)-pyrimidine-2(H)-thione 
• 132131-79-4 5-benzoyl-4-phenyl-1-(2,4,5-trioxo-3-p-tolyl-perhydro-imidazol-1-yl)-pyrimidine-2(H)-thione 
• 132131-77-2 5-benzoyl-4-phenyl-1-(2,4,5-trioxo-3-phenyl-perhydro-imidazol-1-yl)-pyrimidine-2(H)-thione 
• 132131-71-6 1-(5-benzoyl-2-thioxo-4-phenyl-1,2-dihydro-pyrimidine-1-yl)-3-phenyl-urea 
• 1514789-99-1 2,6-bis((E)-((5-benzoyl-2-thioxo-4-phenylpyrimidin-1(2H)-yl)imino)methyl)-4-(methyl)phenol 
• 1361389-67-4 {1-[(5-bromo-2-hydroxybenzylidene)amino]-4-phenyl-2-thioxo-1,2-dihyropyrimidin-5-yl}phenylmethanone 
• 754982-58-6 C₄HN₂(S)(C₆H₅)(C(O)C₆H₅)NCHC₆H₄(OH) 
• 132131-73-8 1-(5-benzoyl-2-thioxo-4-phenyl-1,2-dihydro-pyrimidine-1-yl)-3-p-tolyl-urea 

Relevant academic research and scientific papers

Synthesis, cytotoxic activity and quantum chemical calculations of new 7-thioxopyrazolo[1,5-f]pyrimidin-2-one derivatives

The reactions of 1-amino-2-thioxo-1,2-dihydropyrimidin derivatives 1 and 2 with chloroacetyl chloride in the presence of sodium acetate led to the formation of 7-thioxopyrazolo [1,5-f]pyrimidin-2(1H,3H,7H)-one derivatives (3 and 4) in 78–80% yields. The s

Synthesis, characterisation and antimicrobial activity 1-aminopyrimidine- 2(1H)-thione and its Co(II), Ni(II), Pd(II) and Pt(II) complexes

Metal complexes of 1-aminopyrimidine-2(1H)-thione were prepared from acetate salts of Co(II), Ni(II), Pd(II) and Pt(II) in methanol. Electronic spectral data and magnetic moment measurements suggest mononuclear square planar geometrical structures for the

A Convenient Synthesis of Functionalized 1H-Pyrimidine-2-thiones

The furan-2,3-dione 1 and the thiosemicarbazones 2 combine with loss of carbon dioxide and water yielding the 1-methylenaminopyrimidine-2-thione derivatives 3 in moderate yields (30-60 percent).Their molecular skeleton is confirmed with aid of an X-ray st