1235477-31-2

Basic information

• Product Name: ethyl 2-[[2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)-1-oxoethyl]amino]pentanoate
• Synonyms: ethyl 2-[[2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)-1-oxoethyl]amino]pentanoate
• CAS NO: 1235477-31-2
• Molecular Weight: 429.473
• Mol File: 1235477-31-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2-[[2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)-1-oxoethyl]amino]pentanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-[[2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)-1-oxoethyl]amino]pentanoate(1235477-31-2)
• EPA Substance Registry System: ethyl 2-[[2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)-1-oxoethyl]amino]pentanoate(1235477-31-2)

Safety Data

• Hazardous Substances Data: 1235477-31-2(Hazardous Substances Data)

Upstream product

• 39256-85-4 ethyl 2-amino-L-butyrate 
• 1235477-26-5 2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxopyrimidin-1(2H)-yl)acetic acid 
• 1235477-17-4 ethyl 2-(5-acetyl-3-benzyl-3,4-dihydro-2,4-dioxypyrimidin-1(2H)-yl)acetate 
• 1215293-89-2 3-benzyl-4-imino-2-oxo-1,2,3,4-tetrahydro-5-acetylpyrimidine 

Relevant articles and documents

Synthesis of uracil derivatives and their alkylation: An approach to peptide non-nucleic acid monomers

N3-substituted 5-acetyluracils derived from corresponding N 3-substituted 5-acetylcytosines are versatile functional precursors that allow the introduction of various aliphatic, aromatic, carbocyclic, and carbamoyl functionalities at N1-position. A series of 1,3-disubstituted 5-acetyluracils were synthesized by alkylation at N 1-position. For the introduction of carbamoyl functionalities a convergent approach is studied, leading to N-arylacetamide derivatives; the linear approach furnished peptide non-nucleic acid monomers by replacement of active ester with amino acid esters in good yields.