7615-57-8

Usage

Uses

Used in Material Production:
2,4,6-Tricyano-1,3,5-triazine is used as a precursor in the production of new materials, contributing to the development of innovative substances with potential applications in various industries.
Used in Organic Synthesis:
As a reagent in organic synthesis, 2,4,6-Tricyano-1,3,5-triazine plays a crucial role in the creation of a wide range of chemical compounds, facilitating the advancement of chemical research and product development.
Used in Pharmaceutical Production:
2,4,6-Tricyano-1,3,5-triazine is employed as a chemical intermediate in pharmaceutical production, aiding in the synthesis of biologically active compounds that can be used for the development of new drugs and therapies.
Used in the Synthesis of Biologically Active Compounds:
2,4,6-Tricyano-1,3,5-triazine serves as a building block in the synthesis of biologically active compounds, which can have significant implications in the fields of medicine and healthcare, potentially leading to the discovery of new treatments and therapeutic agents.

InChI:InChI=1/C6N6/c7-1-4-10-5(2-8)12-6(3-9)11-4

Upstream product

• 23297-24-7 1,3,5-triazine tricarbonic acid amide 
• 675-14-9 trifluoro-[1,3,5]triazine 
• 143-33-9 sodium cyanide 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 151-50-8 potassium cyanide 

Downstream Products

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 74-90-8 hydrogen cyanide 
• 108-80-5 isocyanuric acid 
• 460-19-5 ethanedinitrile 

Relevant academic research and scientific papers

Chemical reduction of 2,4,6-tricyano-1,3,5-triazine and 1,3,5-tricyanobenzene. Formation of novel 4,4′,6,6′-tetracyano-2,2′-bitriazine and its radical anion

Chemical reduction of 2,4,6-tricyano-1,3,5-triazine, TCT, results in the formation of an unstable radical anion that undergoes immediate dimerization at a ring carbon to form [C12N12]2-, [TCT]22-, characterized by a long 1.570 (4) A central C - C bond. [TCT]22- can decompose into the radical anion of 4,4′,6,6′-tetracyano-2,2′-bitriazine, [TCBT]-, the one-electron reduced form of planar (D2h) TCBT, which is also structurally characterized as the [TMPD][TCBT] charge-transfer complex (TMPD = N,N,N′,N′-tetramethyl-p-phenylenediamine) with a 1.492 (2) A central sp2 - sp2 C - C bond. Although crystals could not be obtained for the radical anion [TCBT]-, the electrochemistry (E° = +0.03 V), EPR (g = 2.003, 2A14N = 3.347 G, and 4A14N = 0.765 G and a line width of 0.24 G), and theoretical calculations support the formation of [TCBT]-. In addition, thermolysis of [TCT]22- yields [TCBT]-. Chemical reduction of 2,4,6-tricyanobenzene, TCB, forms an unstable radical anion that immediately undergoes dimerization at a ring carbon to form [C12H6N6]2-, [TCB]22-, which has a long 1.560 (5) A central C - C bond. Reaction of TCT with tetrathiafulvalene (TTF) forms structurally characterized [TTF][TCT], and in the presence of water, TCT hydrolyzes to 2,4-dicyano-6-hydroxy-s-triazine, DCTOH. In contrast, the reaction of TCT with TMPD forms [TMPD][TCT], which in the presence of water forms structurally characterized [HTMPD]+[DCTO]-.

Synthesis of linear and hyperbranched tetrazine-based polyhetarylene assemblies with high nitrogen content

The synthesis of polyhetarylenes containing exclusively s-tetrazine and another nitrogen heterocycle (pyridine or s-triazine) is described. The key step involved the polymerization of a suitable di- or triamidrazone, leading to a linear or hyperbranched dihydrotetrazine-based assembly, respectively. The triazinylenetetrazinylene material stands as one of the most nitrogenated polymers ever described.