2,4,6-Tris(trinitromethyl)-1,3,5-triazine
| 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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| Identifiers |
| ChemSpider |
9664224 Y |
| Jmol-3D images |
Image 1 |
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O=[N+]([O-])C(c1nc(nc(n1)C([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O)C([N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O)([N+]([O-])=O)[N+]([O-])=O
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InChI=1S/C6N12O18/c19-10(20)4(11(21)22,12(23)24)1-7-2(5(13(25)26,14(27)28)15(29)30)9-3(8-1)6(16(31)32,17(33)34)18(35)36 Y
Key: MTNISTQLDNOGTM-UHFFFAOYSA-N Y
InChI=1/C6N12O18/c19-10(20)4(11(21)22,12(23)24)1-7-2(5(13(25)26,14(27)28)15(29)30)9-3(8-1)6(16(31)32,17(33)34)18(35)36
Key: MTNISTQLDNOGTM-UHFFFAOYAO
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| Properties |
| Molecular formula |
C6N12O18 |
| Molar mass |
528.13 g/mol |
| Density |
1.91 g/cm³ |
| Melting point |
91–92 °C
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| Related compounds |
| Related compounds |
4,4’-Dinitro-3,3’-diazenofuroxan
Hexanitrohexaazaisowurtzitane
Heptanitrocubane
Octanitrocubane |
Y (verify) (what is: Y/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 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, so could be used 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
- ^ "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