2,4,6-Tris(trinitromethyl)-1,3,5-triazine

2,4,6-Tris(trinitromethyl)-1,3,5-triazine
Names
	IUPAC name 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
Identifiers
CAS Number	161870-33-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	9664224 ;
	InChI 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 Key: MTNISTQLDNOGTM-UHFFFAOYSA-N ; 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;
	SMILES 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;
Properties
Chemical formula	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).
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	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

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. 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. doi:10.1023/A:1023970928207.

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[1] 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. doi:10.1070/MC1995v005n01ABEH000440.

[2] 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. doi:10.1023/A:1023970928207.