Names | |
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Preferred IUPAC name
Tris(trinitromethyl)-1,3,5-triazine | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
PubChem CID |
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Properties | |
C6N12O18 | |
Molar mass | 528.132 g·mol−1 |
Density | 1.91 g/cm3 |
Melting point | 91 to 92 °C (196 to 198 °F; 364 to 365 K) |
Related compounds | |
Related compounds |
4,4’-Dinitro-3,3’-diazenofuroxan Cyanuric triazide Hexanitrohexaazaisowurtzitane Octanitrocubane |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references |
2,4,6-Tris(trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995.[1] It is synthesized 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, thus potentially being useful as an oxygen source, or added to oxygen-poor explosives to increase their power.
Derivatives have been prepared by nucleophilic displacement of the nitro groups with azide and hydrazine.[2]
References
- ↑ Shastin AV, Godovikova TI, Golova SP, Kuz'min VS, Khmel'nitskii LI, Korsunskii BL (1995). "Synthesis of 2,4,6-Tris(trinitromethyl)-1,3,5-triazine". Mendeleev Communications. 5: 17–18. doi:10.1070/MC1995v005n01ABEH000440.
- ↑ Shastin AV, Godovikova TI, Korsunskii BL (2003). "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". Chemistry of Heterocyclic Compounds. 39 (3): 354–356. doi:10.1023/A:1023970928207. S2CID 106383383.
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