1029475-64-6

Basic information

• Product Name: (1-amino-2-thioxo-4-(p-tolyl)-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone
• Synonyms: (1-amino-2-thioxo-4-(p-tolyl)-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone
• CAS NO: 1029475-64-6
• Molecular Weight: 335.429
• Mol File: 1029475-64-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (1-amino-2-thioxo-4-(p-tolyl)-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (1-amino-2-thioxo-4-(p-tolyl)-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone(1029475-64-6)
• EPA Substance Registry System: (1-amino-2-thioxo-4-(p-tolyl)-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone(1029475-64-6)

Safety Data

• Hazardous Substances Data: 1029475-64-6(Hazardous Substances Data)

Upstream product

• 7410-54-0 2-(1-(4-tolyl)ethylidene)hydrazinecarbothioamide 

Downstream Products

• 1180548-89-3 3-(4-methoxybenzoyl)-2-(4-methoxyphenyl)-4-(4-methylbenzoyl)-5-(4-methylphenyl)-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-thione 
• 1180548-93-9 3,4-bis(4-methylbenzoyl)-2,5-bis(4-methylphenyl)-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-thione 
• 1180548-84-8 3-benzoyl-4-(4-methylbenzoyl)-5-(4-methylphenyl)-2-phenyl-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-thione 
• 1180548-80-4 3-acetyl-4-(4-methylbenzoyl)-2-methyl-5-(4-methylphenyl)-3a,6-dihydropyrazolo[1,5-c]pyrimidin-7(3H)-thione 
• 1226645-31-3 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-ethylthiourea 
• 1226645-22-2 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-phenylthiourea 
• 1226645-27-7 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-(3,4-dichlorophenyl)thiourea 
• 1226645-24-4 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-p-methoxyphenylthiourea 
• 1226645-29-9 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-α-naphthylthiourea 
• 1226645-33-5 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-p-nitrophenylthiourea 
• 1226645-25-5 1-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxo-1,2-dihydropyrimidine-1-yl]-3-p-methylphenylthiourea 
• 1333503-37-9 N,N'-bis[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxopyrimidin-1(2H)-yl]ethanediamide 
• 1443640-74-1 N-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxopyrimidine-1(2H)-yl]pyrrolidine-2,5-dione 
• 1443640-76-3 2-[5-(4-methylbenzoyl)-4-(4-methylphenyl)-2-thioxopyrimidine-1(2H)-yl]-1H-isoindole-1,3(2H)-dione 

Relevant articles and documents

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, characterization, and antimicrobial and catalytic activity of a new Schiff base and its metal(II) complexes

We presented the synthesis of a new Schiff base and its complexes properties with some transition metal ions in this study. (1-amino-2-thioxo-4-p-tolyl-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone was synthesized as the starting material, and (1-((2-hydroxynaphthalen-1-yl)methyleneamino)-2-thioxo-4-p-tolyl-1,2-dihydropyrimidin-5-yl)(p-tolyl)methanone (Hnafmmp) (1) and its Ni(II) (2), Pd(II) (3), Pt(II) (4), Cu(II) (5), Co(II) (6) complexes were prepared using above-mentioned starting material. The structures of these new compounds (ligand and its complexes) were characterized with UV–Vis, FTIR, LC–MS, 1H NMR, 13C NMR, magnetic susceptibility, conductivity measurement, X-ray powder diffraction method, and thermal analyses techniques. The 1H NMR chemical shifts of all complexes were calculated by using the gauge-invariant atomic orbital HF (3.21G) method in DMSO phases. All measured results were compared with the experimental data. The ligand and its complexes were also evaluated as antimicrobial agents against representative strains bacteria. Furthermore, we studied the catalytic activity of these compounds in Suzuki–Miyaura cross-coupling reaction in aqueous media.

Reactions of 4-(4-methylbenzoyl)-5-(4-methylphenyl)-2,3-furandione with semi/thiosemi-carbazones

The 4-(4-methylbenzoyl)-5-(4-methylphenyl)-2,3-furandione (1) and various semi-/thiosemicarbazones 2a-h combine with loss of carbondioxide and water yielding 1-methylenaminopyrimidine-2-one and -thione derivatives 3a-h, in moderate yields (43-59%). Hydrol