135264-93-6

Upstream product

• 16947-69-6 2,4,5-Trichlorophenyl chloroformate 
• 81068-69-1 2-(5-fluorouracil-1-yl)-2-(methylthio)ethylamine 
• 16947-68-5 bis(2,4,5-trichlorophenyl) carbonate 
• 95-95-4 2,4,5-trichlorophenol 
• 135264-86-7 N-(2,4,5-trichlorophenoxycarbonyl)imidazole 

Downstream Products

• 81068-92-0 N-<2-(5-fluorouracil-1-yl)-2-(methylthio)ethyl>-N'-cyclohexylurea 
• 134660-36-9 C₁₄H₂₀FN₅O₄S 
• 134660-37-0 2,4,5-trichlorophenyl N-<2-(5-fluorouracil-1-yl)-2-(methylthio)ethyl>-N-nitrosocarbamate 

Relevant academic research and scientific papers

Nucleoside Analogues. Part 11. The Acylation of N-(ω-Aminoalkyl)uracil and a Bicyclic Isomer

The relative reactivity of the amino group and of pyrimidine N1 and N3 in N-(ω-aminoalkyl)uracils has been investigated using a variety of acylating agents.Bis(2,4,5-trichlorophenyl) carbonate, now readily available from bis(trichloromethyl) carbonate, proved a very useful selective reagent.The bicyclic isomer formed from an N1-substituted compound by intramolecular addition was also studied and afforded novel products from 2,4,5-trichlorophenyl N-(2-chloroethyl)-N-nitrosocarbamate, a standard reagent for producing N-nitrosoureas.