Application of cas: 18592-13-7 | Sugiyama, N. et al. published an article in 2008

6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione (cas: 18592-13-7 Recommanded Product: 6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione) 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.

Recommanded Product: 6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione《Molecular recognition of Langmuir-Blodgett polymer films containing uracil groups》 was published in 2008. The authors were Sugiyama, N.;Hirakawa, M.;Zhu, H.;Takeoka, Y.;Rikukawa, M., and the article was included in《Colloids and Surfaces, A: Physicochemical and Engineering Aspects》. The author mentioned the following in the article:

Novel copolymers, poly(acryroyloxymethyluracil-co-hexylacrylamide)s (poly(AU-co-HAAm)s), were synthesized by radical copolymerization with different monomer ratios. The poly(AU-co-HAAm)s formed stable monolayers at the air-water interface and could be deposited on solid substrates as Y-type films by the vertical dipping method. The mol. structure of poly(AU-co-HAAm) LB films was determined by reflection absorption and transmission FTIR, and x-ray diffraction measurements. Evidence for preferential orientation of both the AU and HAAm units was found. The LB films deposited on quartz crystal microbalance substrates adsorbed adenosine mols., and the adsorbed amounts increased with higher contents of uracil groups in poly(AU-co-HAAm)s. Some morphol. changes of LB films were also observed by at. force microscopy (AFM) after the mol. recognition.6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione (cas: 18592-13-7) were involved in the experimental procedure.

6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione (cas: 18592-13-7 Recommanded Product: 6-(Chloromethyl)pyrimidine-2,4(1H,3H)-dione) 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