108047-30-9

Basic information

• Product Name: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil
• Synonyms: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil
• CAS NO: 108047-30-9
• Molecular Weight: 292.208
• Mol File: 108047-30-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil(CAS DataBase Reference)
• NIST Chemistry Reference: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil(108047-30-9)
• EPA Substance Registry System: 3-methyl-5-nitro-1-(p-nitrophenyl)uracil(108047-30-9)

Safety Data

• Hazardous Substances Data: 108047-30-9(Hazardous Substances Data)

Upstream product

• 125236-31-9 1-(4-nitro-phenyl)-1H-pyrimidine-2,4-dione 
• 350-46-9 4-Fluoronitrobenzene 
• 128039-16-7 3-methyl-1-(p-nitrophenyl)uracil 
• 37721-30-5 3-methyl-1-phenyluracil 
• 128039-12-3 1-methyl-1-(3-methylamino-2-nitroacryloyl)-3-(p-nitro-phenyl)urea methylammonium salt 
• 934802-64-9 3-methyl-5-nitro-1-phenyluracil 

Downstream Products

• 78999-59-4 1-cyclohexyl-3-methyl-5-nitrouracil 
• 108070-70-8 5,6-dihydro-3-methyl-6-methylamino-1-(p-nirophenyl)uracil methylammonium salt 
• 128039-12-3 1-methyl-1-(3-methylamino-2-nitroacryloyl)-3-(p-nitro-phenyl)urea methylammonium salt 
• 41613-26-7 1,3-dimethyl-5-nitrouracil 
• 100-01-6 4-nitro-aniline 
• 128039-14-5 1-(3-dimethylamino-2-nitroacryloyl)-1-methyl-3-(p-nitrophenyl)urea 
• 128039-13-4 5,6-dihydro-3-methyl-5-nitro-1-(p-nitrophenyl)uracil 
• 25912-37-2 3-methyl-5-nitro-2,4(1H,3H)pyrimidinedione 

Relevant articles and documents

N-Functionalization of uracil derivatives: Synthesis of chiral 2-(3-methyl-5-nitro-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)alkanoic acids and their methyl esters

3-Methyl-5-nitro-1-(4-nitrophenyl)uracil has been obtained by regioselective arylation of uracil using 4-nitrofluorobenzene, followed by methylation at the nitrogen atom N-3 and subsequent nitration of the uracil ring. 3-Methyl-5-nitro-1-(4-nitrophenyl)ur

Novel Reaction of Uracil Derivatives Possessing Electron-withdrawing Groups at the 5-Position with Amines: Exchange Reaction between the N1-Portion of Uracils and Amines

The reaction of 1,3-disubstituted uracils possessing an electron-withdrawing group such as nitro, carbamoyl, and cyano at 5-position with primary amines resulted in the exchange of the N1-portion of the uracil ring with the amine moiety.The exchange reactions were influenced by the nature of substituents at the 5- and N1-position.The reaction sequence is explained in terms of addition, ring-opening, and ring-closure.