74966-63-5

Upstream product

• 108-94-1 cyclohexanone 
• 670-54-2 ethenetetracarbonitrile 

Downstream Products

• 95059-27-1 9-Imino-12-(3-nitro-phenyl)-10,11-dioxa-tricyclo[6.2.2.0^1,6]dodecane-7,7,8-tricarbonitrile 
• 95059-26-0 9-Imino-12-phenyl-10,11-dioxa-tricyclo[6.2.2.0^1,6]dodecane-7,7,8-tricarbonitrile 
• 97866-28-9 3-(1-propenyl)-4,5,5-tricyano-12-imino-2,11-dioxatricyclo<4.2.2.2^1,4>dodecane 
• 185459-62-5 5,6-tetramethylene-2-phenyl-1,2,3,4-tetrahydropyridine-3,3,4,4-tetracarbonitrile 
• 185459-99-8 5,6-tetramethylene-3,3,4-tricyano-2-phenyl-2,3,4,5-tetrahydropyridine-4-carboxamide 
• 185460-03-1 3-amino-6,7-tetramethylene-1-oxo-4-phenyl-3a,4,5,7a-tetrahydro-1H-pyrrolo[3,4-c]pyridine-3a,7a-dicarbonitrile 
• 1346229-61-5 5-amino-2-(morpholin-4-yl)-3-(2-oxocyclohexyl)-3H-pyrrol-3,4-dicarbonitrile 
• 1515847-83-2 3a-(2-oxocyclohexyl)pyrrolo[3,4-c]pyrrole-1,3,4,6(2H,3aH,5H,6aH)-tetraone 

Relevant academic research and scientific papers

Regiospecific synthesis of gem-dinitro derivatives of 2-halogenocycloalka[b]pyridine-3,4-dicarbonitriles

Abstract A simple method for the synthesis of inaccessible gem-dinitro derivatives of pyridine is described. A wide range of 2-halogencycloalka[b]pyridine-3,4-dicarbonitriles are produced by the three-component reaction (ketone, TCNE, hydrohalic acid), si

Glycine catalyzed diastereoselective domino-synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles in water

The first example of glycine-catalyzed direct domino synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]octane-4,4,5-tricarbonitriles in aqueous medium is described, giving products in excellent yields and moderate to excellent diastereoselectivities. This appro

Novel chromophores of cyanopyridine series with strong solvatochromism and near-infrared solid-state fluorescence

A series of novel pyridine derivatives containing tetracyanobutadiene moiety (4-CN-TCPy) were obtained in good yields by the reaction of 2-chlorosubstituted pyridine-3,4-dicarbonitriles with malononitrile using Cs2CO3 as a catalyst.

Rearrangement of 4-oxobutane-1,1,2,2-tetracarbonitriles to the penta-1,3-diene-1,1,3-tricarbonitrile moiety as an approach to novel acceptors for donor–acceptor chromophores

The rearrangement of 4-oxobutane-1,1,2,2-tetracarbonitriles to give the penta-1,3-diene-1,1,3-tricarbonitrile moiety, accompanied by elongation of the carbon chain via introduction of the cyano group carbon atom to the carbon skeleton, is described. The r

Ene-Type Reaction through the Intermediacy of the 1,4-Dipolar Ion in the Reaction of Tetracyanoethylene with Nucleophilic Double Bonds in Liquid Sulfur Dioxide

The expected cycloadduct from the reaction of tetracyanoethylene with 1-methoxycyclohexene in liquid sulfur dioxide underwent a previously unrecognized reaction to give 1-methoxy-6-(1,1,2,2-tetracyanoethyl)-cyclohexene.Further isomerization of thi