2,4,6-Tris(trinitromethyl)-1,3,5-triazine
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2,4,6-Tris(trinitromethyl)-1,3,5-triazine | |
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IUPAC name | 2,4,6-Tris(trinitromethyl)-1,3,5-triazine |
Identifiers | |
CAS number | xx-xx-xx |
SMILES | xxx |
Properties | |
Molecular formula | C6N12O18 |
Molar mass | 528.13 g/mol |
Density | 1.91 g/cm³ |
Melting point |
91-92 °C |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
2,4,6-Tris(trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995. It is synthesised by destructive nitration of 2,4,6-tricarboxyl-1,3,5-triazine. It is noteworthy for having more nitro groups than it does carbon atoms, so could be used as an oxygen source, or added to oxygen-poor explosives to increase their power.
[edit] References
The references in this article would be clearer with a different or consistent style of citation, footnoting, or external linking. |
- "Synthesis of 2,4,6-Tris(trinitromethyl)-1,3,5-triazine", Alexey V Shastin, Tamara I Godovikova, Svetlana P Golova, Vladimir S Kuz'min, Lenor I Khmel'nitskii, Boris L Korsunskii, Mendeleev Communications; Volume 5 (1995), Number 1, Pages 17-18 Abstract
- "Nucleophilic Substitution Reactions of 2,4,6-Tris(trinitromethyl)-1,3,5-triazine. 3. Reaction of 2,4,6-Tris(trinitromethyl)-1,3,5-triazine with Azides and Hydrazine", A. V. Shastin, T. I. Godovikova and B. L. Korsunskii. Chemistry of Heterocyclic Compounds, March 2003; 39(3): 354-356. Abstract