161970-50-9

Upstream product

• 50-00-0 formaldehyd 
• 119-62-0 (1S,2S)-2-amino-1-(4-nitrophenyl)propane-1,3-diol 

Downstream Products

• 900797-83-3 2,4-dichloro-6-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 1042072-73-0 2,4-di(diethylamino)-6-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 1042072-75-2 2-(diethylamino)-4,6-bis{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 1042072-87-6 2,4,6-tris{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 1042072-77-4 2-chloro-4-(diethylamino)-6-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 1201651-69-5 2-chloro-6-{[1,3-dihydroxy-2-(hydroxymethyl)prop-2-yl]amino}-4-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazine 
• 1414965-72-2 1-{6-{[1-hydroxy-2-(hydroxymethyl)but-2-yl]amino}-4-{[(4S,5S)-4-(4-nitrophenyl)-1,3-dioxan-5-yl]amino}-s-triazin-2-yl}piperazine 

Relevant academic research and scientific papers

New serinolic amino-s-triazines by chemoselective amination of cyanuric chloride and their (pro)diastereomerism in restricted rotational phenomena

The highly chemoselective preparation of new elaborated N-unsymmetrically substituted chlorodiamino-s-triazines and melamines, seen as building-blocks for iterative synthesis, is reported. It consisted of amination of cyanuric chloride with commercial C-2

Serinolic amino-s-triazines: Iterative synthesis of N-substituted amino-1,3-dioxane derivatives from l-(p-nitrophenyl)serinols and rotational stereochemistry phenomena

We report the first iterative and chemioselective approach towards the synthesis of highly elaborated N-substituted 2,4,6-triamino-s-triazines (melamines) and precursors, by amination of cyanuric chloride with anancomeric and enantiomerically pure primary