Study of the dependence of the reactivity of substituted dichloro-s-triazines on the nature of the substituent was written by Smirnova, O. V.;Bolmosova, V. P.;Kutepov, D. F.;Eryshev, B. Ya.. And the article was included in Zhurnal Prikladnoi Khimii in 1979.Synthetic Route of C9H6Cl2N4 The following contents are mentioned in the article:
Substituents having π-π, π-p, or π-p-π conjugation with the triazine ring increase its basicity and decrease its rate of nucleophilic substitution in polycondensation with bisphenol A [80-05-7]. Rate constants for the polymerization of 2-substituted 4,6-dichloro-1,3,5-triazines with bisphenol A increase in the substituent order: Ph < piperidyl < NHPh < NPh2. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Synthetic Route of C9H6Cl2N4).
4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Synthetic Route of C9H6Cl2N4
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics