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・ 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

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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.〔"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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