Mather, Brian D.;Lizotte, Jeremy R.;Long, Timothy E. published 《Synthesis of end functional multiple hydrogen bonded polystyrenes and poly(alkyl acrylates) using controlled radical polymerization》. The research results were published in《Polymer Preprints (American Chemical Society, Division of Polymer Chemistry)》 in 2004.HPLC of Formula: 18592-13-7 The article conveys some information:
Uracil-containing alkoxyamines involving both TEMPO and N-tert-butyl-N-(1-diethylphosphono-2,2-dimethylpropyl) nitroxide (DEPN) were synthesized and used in the stable free radical polymerization of styrene and Bu acrylate. The resultant polymers exhibited narrow mol. weight distributions (Mw/Mn ∼1.20) and controlled mol. weights characteristic of stable free radical polymerizations Characterization of the polymers using proton NMR spectroscopy and melt rheol. demonstrated the presence of the hydrogen bonding interaction. The experimental procedure involved many compounds, such as 6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione (cas: 18592-13-7) .
6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione (cas: 18592-13-7 HPLC of Formula: 18592-13-7) was used in the synthesis of: 5-bromo-6-(chloromethyl)uracil, pteridine compounds, potential anticancer agents, substituted uracil pyridinium compounds, potential inhibitors of thymidine phosphorylase.
Reference:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia