41949-07-9

Upstream product

• 874-14-6 1,3-dimethyluracil 
• 139958-85-3 6-hydroxy-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidine-5-carbaldehyde 
• 89-25-8 edaravone 

Downstream Products

• 69310-69-6 1,3-dimethyl-2,4-dioxo-7-phenyl-1,3,4,5,6,7-hexahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylic acid ethyl ester 
• 37470-98-7 1,3-dimethyl-6,7-diphenyl-1,5,6,7-tetrahydro-pyrano[2,3-d]pyrimidine-2,4-dione 
• 53746-86-4 1,3-dimethyl-5-(4'-oxo-6,6'-diphenyl-4'H-[2,2']bipyranyl-4-ylidene)-pyrimidine-2,4,6-trione 
• 54112-17-3 1,3,1',3'-tetramethyl-5,5'-(6,6'-diphenyl-[2,2']bipyranyl-4,4'-diylidene)-bis-pyrimidine-2,4,6-trione 
• 1005789-33-2 1-tert-butyl-3,4-diphenyl-1,2,4-triazolium 1,3-dimethylbarbiturate 
• 34654-80-3 1,3-dimethyl-6-(3-hydroxy-propyl)amino uracil 
• 1257244-45-3 5-(4-fluorophenyl)-1,3,8,8-tetramethyl-8,9-dihydro-1H-chromeno[2,3-d]pyrimidine-2,4,6(3H,5H,7H)-trione 
• 1257244-51-1 5-(4-methylphenyl)-1,3,8,8-tetramethyl-8,9-dihydro-1H-chromeno[2,3-d]pyrimidine-2,4,6(3H,5H,7H)-trione 
• 1257244-47-5 5-(4-methoxyphenyl)-1,3,8,8-tetramethyl-8,9-dihydro-1H-chromeno[2,3-d]pyrimidine-2,4,6(3H,5H,7H)-trione 
• 1251930-57-0 1,3,8,8-tetramethyl-5-(4-nitrophenyl)-8,9-dihydro-1H-chromeno[2,3-d]pyrimidine-2,4,6(3H,5H,7H)-trione 
• 1251930-61-6 5-(4-bromophenyl)-1,3,8,8-tetramethyl-8,9-dihydro-1H-chromeno[2,3-d]pyrimidine-2,4,6(3H,5H,7H)-trione 
• 380194-46-7 7?amino?5?(2,4?dichlorophenyl)?1,3?dimethyl?2,4?dioxo?1,3,4,5?tetrahydro?2H?pyrano[2,3?d]pyrimidine?6?carbonitrile 
• 1072002-79-9 7-amino-1,3-dimethyl-5-(3-nitrophenyl)-2,4-dioxo-1,3,4,5-tetrahydro-2H-pyrano [2,3-d]pyrimidine-6-carbonitrile 
• 1429128-28-8 1,3-dimethyl-5-(1-(methylamino)-2-oxo-2-phenylethylidene)pyrimidine-2,4,6(1H,3H,5H)-trione 

Relevant academic research and scientific papers

A mild and efficient method for the deformylation of 5-formyl uracils and synthesis of 4,4￠-methylidenebis(1-phenyl-3-methyl-5-pyrazolone)

6-Substituted 5-formyl uracils undergo an interesting reaction with 1-phenyl-3-methyl-5-pyrazolone in the presence of base catalyst to afford deformylated uracils and 4,4￠-methylidenebis(1-phenyl-3-methyl-5- pyrazolone) in excellent yields. Georg Thieme V

Oxidation of 1,3-dimethylthymine and 1,3-dimethyluracil with oxone in the solid to solid state

The oxidation of the title substrates with Oxone in the presence of camphor in the solid to solid state afforded a simple and efficient method for epoxidation under mild reaction condition.