Abstract
The title compound, C 17 H 16 N 4 O 2 , was synthesized by the reaction of 4,6-dichloro-1,3,5-triazin-2-ylamine, obtained from cyanuric chloride, with powdered sodium hydroxide in benzyl alcohol. It crystallizes as a centrosymmetric hydrogen-bonded dimer, with only one of the two H atoms of the amino group involved in a hydrogen bond. Whereas one of the two phenyl rings is nearly coplanar with the triazine ring, the other one is nearly perpendicular to it.
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