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1,3,5-Triazine-2,4,6-tricarbonitrile

Base Information
  • Chemical Name:1,3,5-Triazine-2,4,6-tricarbonitrile
  • CAS No.:7615-57-8
  • Molecular Formula:C6N6
  • Molecular Weight:156.106
  • Hs Code.:
  • European Community (EC) Number:854-093-5
  • DSSTox Substance ID:DTXSID00274764
  • Nikkaji Number:J14.738I
  • Wikidata:Q82004217
  • Mol file:7615-57-8.mol
1,3,5-Triazine-2,4,6-tricarbonitrile

Synonyms:1,3,5-triazine-2,4,6-tricarbonitrile;7615-57-8;2,4,6-Tricyano-1,3,5-triazine;S-TRIAZINE-2,4,6-TRICARBONITRILE;Hexacyanogen;Tricyan-sym-triazin;DTXSID00274764;1,3,5-Triazine, 2,4,6-tricarbonitrile;FT-0738908;EN300-2486194;Z1255358237

Suppliers and Price of 1,3,5-Triazine-2,4,6-tricarbonitrile
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 49 raw suppliers
Chemical Property of 1,3,5-Triazine-2,4,6-tricarbonitrile
Chemical Property:
  • Vapor Pressure:9.18E-08mmHg at 25°C 
  • Melting Point:119°C 
  • Refractive Index:1.6020 (estimate) 
  • Boiling Point:434.8°Cat760mmHg 
  • PKA:-7.26±0.10(Predicted) 
  • Flash Point:141.4°C 
  • PSA:110.04000 
  • Density:1.58g/cm3 
  • LogP:-0.51336 
  • XLogP3:0.1
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:0
  • Exact Mass:156.01844403
  • Heavy Atom Count:12
  • Complexity:242
Purity/Quality:

97% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C(#N)C1=NC(=NC(=N1)C#N)C#N
  • General Description 2,4,6-Tricyano-1,3,5-triazine (TCT) undergoes chemical reduction to form an unstable radical anion that dimerizes into [TCT]22-, characterized by a long central C–C bond (1.570 ?). This dimer can decompose into the radical anion of 4,4′,6,6′-tetracyano-2,2′-bitriazine ([TCBT]-), which exhibits planar geometry and is stabilized in charge-transfer complexes. Additionally, TCT reacts with tetrathiafulvalene (TTF) to form [TTF][TCT] and hydrolyzes in water to yield 2,4-dicyano-6-hydroxy-s-triazine (DCTOH). Its reactivity with N,N,N′,N′-tetramethyl-p-phenylenediamine (TMPD) produces [TMPD][TCT], which further hydrolyzes to form [HTMPD]+[DCTO]-.
Technology Process of 1,3,5-Triazine-2,4,6-tricarbonitrile

There total 5 articles about 1,3,5-Triazine-2,4,6-tricarbonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In acetonitrile; at 20 ℃; for 40h;
DOI:10.1021/jo025833h
Guidance literature:
In acetonitrile; at 0 - 15 ℃; for 21h;
DOI:10.1016/j.tet.2007.07.097
Guidance literature:
With phosphorus pentaoxide; at 210 - 250 ℃;
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