77778-41-7

Basic information

• Product Name: 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-[(4-bromophenyl)methylamino]-3-methyl-
• CAS NO: 77778-41-7
• Molecular Formula: C12H11Br2N3O2
• Molecular Weight: 389.046
• Mol File: 77778-41-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-[(4-bromophenyl)methylamino]-3-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-[(4-bromophenyl)methylamino]-3-methyl-(77778-41-7)
• EPA Substance Registry System: 2,4(1H,3H)-Pyrimidinedione, 5-bromo-6-[(4-bromophenyl)methylamino]-3-methyl-(77778-41-7)

Safety Data

• Hazardous Substances Data: 77778-41-7(Hazardous Substances Data)

Upstream product

• 36995-90-1 3-methyl-6-(N-methylanilino)uracil 
• 64455-88-5 3-methyl-6-(N-methyl-p-bromoanilino)uracil 

Downstream Products

• 64455-88-5 3-methyl-6-(N-methyl-p-bromoanilino)uracil 
• 63955-66-8 1,1′-dimethyl-1H,1′H-2,3′-biindole 
• 91167-04-3 3-methyl-6-(N-methyl-p-bromoanilino)-5-(p-toluidino)pyrimidine-2,4(1H,3H)-dione 

Relevant articles and documents

Reductive Debromination and Coupling Reaction in the Thermolysis of 5-Bromouracils in N,N-Dialkylamides. Cleavage of the C(5)-Bromine bond by an Initial Electron-transfer Process

Thermolysis of various 5-bromouracils (1) in N,N-dialkylamides results in the formation of methylenebisuracils (2) and reductive debrominated products (3) via cleavage of the C(5)-Br bond; the latter involves a one-electron transfer process.The product distribution between (2) and (3) depends upon the nature of substituents in the uracil ring.