De Bie, Dick A. published the artcilePhotoreactivity of diazines. III. Pyrimidines. XXXVIII. Photoamination of halopyrimidines, Quality Control of 41270-96-6, the publication is Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) (1974), 1363-5, database is CAplus.
4-Amino-6-phenylpyrimidine was prepared by uv-induced amination of 4-halo-6-phenylpyrimidines in liquid NH3. A pyrimidinyl radical was formed by cleavage of C-halogen bonds. The order of reactivity was I > Br > Cl. 4-Phenylpyrimidine was also formed from the iodo and bromo compounds
Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) published new progress about 41270-96-6. 41270-96-6 belongs to iodides-buliding-blocks, auxiliary class Pyrimidine,Iodide,Benzene,Immunology/Inflammation,MIF, name is 4-Iodo-6-phenylpyrimidine, and the molecular formula is C10H7IN2, Quality Control of 41270-96-6.
Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com