Study of the properties of some triazine-containing polycarbonates was written by Smirnova, O. V.;Kutepov, D. F.;Bolmosova, V. P.;Atrushkevich, A. A.. And the article was included in Trudy Instituta – Moskovskii Khimiko-Tekhnologicheskii Institut imeni D. I. Mendeleeva in 1980.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:
I (R = Ph, NPh2, NHPh, or piperidino; m = 5-30; 2m + n = 100) showed higher alkali resistance and O index and lower thermal stability in comparison with Diflon [24936-68-3] (I, m = 0). The thermal degradation of I was presumed to proceed via homolytic cleavage of the C-N bonds of the triazine rings, based on high (>167.6 kJ/mol) activation energies of liberation of CO2, CO, and CH4 gases from I and model compounds The thermal degradation of I began at 300-310, 290, and 265-290° for m = 0, 5, and 30, resp., while thermal stability of I (m = 30) decreased in the order: R = Ph, NPh2, NHPh, and piperidino. The alkali resistance of I increased with decreasing NaOH solution concentration and exposure period and with increasing m. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine).
4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Quality Control of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics