2,4,6-Tris(trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995. 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.
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| - 2,4,6-Tris(trinitromethyl)-1,3,5-triazine (en)
- 2,4,6-三(三硝基甲基)-1,3,5-三嗪 (zh)
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| - 2,4,6-Tris(trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995. 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. (en)
- 2,4,6-三(三硝基甲基)-1,3,5-三嗪是一种三嗪的衍生物,最早于1995年制得。 它由2,4,6-三羧基-1,3,5-三嗪的破坏性硝化反应制得。值得注意的是,其中的硝基数目比碳原子数目还多,因此可以作为氧的来源,或者添加到含氧较少的炸药中来增强它们的威力。 通过叠氮化物或肼的亲核取代反应可以替换硝基而制得它的衍生物。 (zh)
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| - 2,4,6-Tris(trinitromethyl)-1,3,5-triazine (en)
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| - 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
- 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
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| - 246 (xsd:integer)
- Ball-and-stick model of the 2,4,6-tris-1,3,5-triazine molecule (en)
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| - 2,4,6-Tris(trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995. 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. (en)
- 2,4,6-三(三硝基甲基)-1,3,5-三嗪是一种三嗪的衍生物,最早于1995年制得。 它由2,4,6-三羧基-1,3,5-三嗪的破坏性硝化反应制得。值得注意的是,其中的硝基数目比碳原子数目还多,因此可以作为氧的来源,或者添加到含氧较少的炸药中来增强它们的威力。 通过叠氮化物或肼的亲核取代反应可以替换硝基而制得它的衍生物。 (zh)
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| - Tris(trinitromethyl)-1,3,5-triazine (en)
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