Chemistry:4,4'-Dinitro-3,3'-diazenofuroxan
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IUPAC name
(E)-4-Nitro-N-[(E)-(4-nitro-2-oxo-1,2,5-oxadiazol-2-ium-3-ylidene)amino]-2-oxido-1,2,5-oxadiazol-3-imine
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Other names
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3D model (JSmol)
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Properties | |
C4N8O8 | |
Molar mass | 288.092 g/mol |
Density | 2.02 g/cm3 |
Hazards | |
Main hazards | Highly Explosive |
Explosive data | |
Detonation velocity | 10,000 m/s |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Tracking categories (test):
4,4’-Dinitro-3,3’-diazenofuroxan (DDF) is a powerful experimental high explosive with performance comparable to that of other high-density high-explosives such as octanitrocubane. It is synthesised by oxidative coupling of 4-amino-3-(azidocarbonyl)furoxan followed by Curtius rearrangement and further oxidation.[1][2]
See also
- 3,3′‐Diamino‐4,4′‐azoxyfurazan (DAAF)
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- ONC
- Octaazacubane (N8)
- Hexanitrobenzene (HNB)
- Hexanitrohexaazaisowurtzitane (HNIW)
- HNC
- HHTDD
References
- ↑ "4-Amino-3-azidocarbonyl Furoxan as an Universal Synthon for the Synthesis of Energetic Compounds of the Furoxan Series.". 30th International Annual Conference of ICT. Karlsruhe, Germany. 1999. pp. 58/1–58/10.
- ↑ Organic Chemistry of Explosives. John Wiley & Sons Ltd. 2007. p. 303. ISBN 978-0-470-02967-1.
Original source: https://en.wikipedia.org/wiki/4,4'-Dinitro-3,3'-diazenofuroxan.
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