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

Names
Preferred IUPAC name Tris(trinitromethyl)-1,3,5-triazine
Identifiers
CAS Number	161870-33-3 Y
3D model (JSmol)	Interactive image
ChemSpider	9664224 Y
PubChem CID	11489412
CompTox Dashboard (EPA)	DTXSID901027076
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 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
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). N verify (what is YN ?) 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]