翻訳と辞書 ・ 2,4'-dihydroxyacetophenone dioxygenase ・ 2,4,5-Trichlorophenoxyacetic acid ・ 2,4,5-Trihydroxyamphetamine ・ 2,4,5-Trihydroxycinnamic acid ・ 2,4,5-Trihydroxymethamphetamine ・ 2,4,5-Trimethoxyphenethylamine ・ 2,4,5-Trimethoxypropiophenone ・ 2,4,6-Tribromoanisole ・ 2,4,6-Tribromophenol ・ 2,4,6-Trichloroanisole ・ 2,4,6-Trichlorophenol ・ 2,4,6-Trihydroxyacetophenone ・ 2,4,6-Trimethylaniline ・ 2,4,6-Trinitroaniline ・ 2,4,6-Trinitrobenzenesulfonic acid ・ 2,4,6-Tris(trinitromethyl)-1,3,5-triazine ・ 2,4,7-trihydroxy-1,4-benzoxazin-3-one-glucoside 7-O-methyltransferase ・ 2,4-Bis(4-hydroxybenzyl)phenol ・ 2,4-DB ・ 2,4-Diacetylphloroglucinol ・ 2,4-diaminopentanoate dehydrogenase ・ 2,4-Diaminopyrimidine ・ 2,4-Diaminotoluene ・ 2,4-dichlorobenzoyl-CoA reductase ・ 2,4-Dichlorobenzyl alcohol ・ 2,4-Dichlorophenol ・ 2,4-dichlorophenol 6-monooxygenase ・ 2,4-Dichlorophenoxyacetic acid ・ 2,4-Dihydroxy-1,4-benzoxazin-3-one-glucoside dioxygenase ・ 2,4-Dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one 2 -D-glucosyltransferase
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2,4,6-Tris(trinitromethyl)-1,3,5-triazine : ウィキペディア英語版 | 2,4,6-Tris(trinitromethyl)-1,3,5-triazine
|Section2= |Section8= }} 2,4,6-Tris(trinitromethyl)-1,3,5-triazine is a chemical compound that is a derivative of triazine first prepared in 1995.〔"Synthesis of 2,4,6-Tris(trinitromethyl)-1,3,5-triazine", Alexey V Shastin, Tamara I Godovikova, Svetlana P Golova, Vladimir S Kuz'min, Lenor I Khmel'nitskii, Boris L Korsunskii, Mendeleev Communications; Volume 5 (1995), Number 1, Pages 17–18 (Abstract )〕 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.〔"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", A. V. Shastin, T. I. Godovikova and B. L. Korsunskii. Chemistry of Heterocyclic Compounds, March 2003; 39(3): 354-356. (Abstract )〕 ==References==
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