1518987-34-2

Basic information

• Product Name: 5-(4-bromophenethyl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione
• Synonyms: 5-(4-bromophenethyl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione
• CAS NO: 1518987-34-2
• Molecular Weight: 353.216
• Mol File: 1518987-34-2.mol

Chemical Properties

• CAS DataBase Reference: 5-(4-bromophenethyl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-bromophenethyl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione(1518987-34-2)
• EPA Substance Registry System: 5-(4-bromophenethyl)-1,3,5-trimethylpyrimidine-2,4,6(1H,3H,5H)-trione(1518987-34-2)

Safety Data

• Hazardous Substances Data: 1518987-34-2(Hazardous Substances Data)

Upstream product

• 74-88-4 methyl iodide 

Relevant articles and documents

Stereoselective capture of n-acyliminium ions generated from a-hydroxy-n-acylcarbamides: Direct synthesis of uracils from barbituric acids enabled by smi2 reduction

Lewis acid promoted cleavage of a-amino alcohols derived from barbituric acids via chemoselective Sm(II)-mediated electron transfer affords a wide range of C6-substituted 5,6-dihydrouracils. The reaction involves the first generation of Nacyliminium ions