2112-21-2

Upstream product

• 118-96-7 2,4,6-Trinitrotoluene 
• 37841-25-1 1-cyano-2,4,6-trinitrobenzene 
• 2213-80-1 1,2-dichloro-3,5-dinitrobenzene 
• 544-92-3 copper(I) cyanide 

Downstream Products

• 97112-86-2 2-Amino-6-chloro-4-piperidin-1-yl-benzonitrile 
• 97112-85-1 2-Amino-6-chloro-4-dimethylamino-benzonitrile 
• 97112-72-6 2-Chloro-4-dimethylamino-6-nitro-benzonitrile 
• 97112-73-7 2-Chloro-6-nitro-4-piperidin-1-yl-benzonitrile 

Relevant academic research and scientific papers

Chemistry of 2,4,6-trinitrobenzonitrile 1. Nitro group substitution in 2,4,6-trinitrobenzonitrile under the action of anionic nucleophiles. Factors favoring substitution of the ortho-nitro group

The direction of the nitro group substitution (the ratio of the ortho/para substitution) in 2,4,6-trinitrobenzonitrile under the action of anionic nucleophiles (MeO-, RS-, and N3-) as well as of HCl was studied.

Reactivity of Activated Methylene Group in Nitro Compounds. III. Formation of 2,4,6-Trinitrobenzonitrile in the Reaction of 2,4,6-Trinitrotoluene with Carboxylic Acid Chlorides and Anhydrides

With the reactions of 2,4,6-trinitrotoluene with carboxylic acid chlorides and anhydrides in the presence of pyridine as examples we showed for the first time that nitrogen atom of a nitro group can be involved in formation of a cyano group.

Cyclic guanidines. 17. Novel (N-substituted amino)imidazo[2,1-b]quinazolin-2-ones: Water-soluble platelet aggregation inhibitors

A series of novel 1,2,3,5-tetrahydroimidazo[2,1-b]quinazolin-2-one derivatives substituted with a secondary amino group has been prepared and tested for the activities of inhibiting platelet aggregation in rats in vitro and ex vivo. Most of the compounds