4,4'-Dinitro-3,3'-diazenofuroxan
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Names | |
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IUPAC name
4,4’-dinitro-3,3’-diazenofuroxan
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Other names
DDF
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Identifiers | |
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Properties | |
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Molar mass | 288.092 g/mol |
Density | 2.02 g/cm3 |
Vapor pressure | {{{value}}} |
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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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Infobox references | |
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
References
- ↑ Binnikov AN, Kulikov AS, Makhova NN, Ovchinnikov IV, Pivina TS. 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. 58/1–58/10.
- ↑ Agrawal JP, Hodgson RD. Organic Chemistry of Explosives. John Wiley & Sons Ltd, 2007. p303. ISBN 978-0-470-02967-1
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