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Vedachalam, Murugappa; Ramakrishnan, Vayalakkavoor T.; Boyer, Joseph H.; Dagley, Ian J.; Nelson, Keith A.; Adolph, Horst G.; Gilardi, Richard; George, Clifford; Flippen-Anderson, Judith L. (1991). "Facile synthesis and nitration of cis-syn-cis-2,6-dioxodecahydro-1H,5H-diimidazopyrazine".
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even higher than that of CL-20, HHTDD readily decomposes in the presence of even trace amounts of water, making it unsuitable for any practical applications.
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InChI=1S/C6H4N12O14/c19-5-9(15(25)26)1-2(10(5)16(27)28)8(14(23)24)4-3(7(1)13(21)22)11(17(29)30)6(20)12(4)18(31)32/h1-4H
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InChI=1/C6H4N12O14/c19-5-9(15(25)26)1-2(10(5)16(27)28)8(14(23)24)4-3(7(1)13(21)22)11(17(29)30)6(20)12(4)18(31)32/h1-4H
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compound. It is essentially an open analogue of the cyclic nitroamine cage compounds such as
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Except where otherwise noted, data are given for materials in their
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C12C(N(C3C(N1(=O))N(C(=O)N3(=O))(=O))(=O))N(C(=O)N2(=O))(=O)
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1,3,4,5,7,8-Hexanitrooctahydrodiimidazopyrazine-2,6(1
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398:2,4,6-Tris(trinitromethyl)-1,3,5-triazine
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379:. While it is highly explosive, with a
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58:Hexanitrohexaazatricyclododecanedione
369:hexanitrohexaazatricyclododecanedione
213:Key: ZFBXJPJQJKATGM-UHFFFAOYSA-N
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223:Key: ZFBXJPJQJKATGM-UHFFFAOYAE
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486:. You can help Knowledge (XXG) by
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441:The Journal of Organic Chemistry
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326:(at 25 °C , 100 kPa).
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482:-related article is a
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37:Preferred IUPAC name
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447:(10): 3413–3419.
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68:Identifiers
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96:3D model (
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419:RE factor
373:explosive
316:9700 m/s
387:See also
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129:23078717
346:what is
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141:PubChem
49:)-dione
341:verify
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237:SMILES
60:DTNGU
31:Names
17:HHTDD
478:This
405:(DDF)
377:CL-20
365:HHTDD
202:InChI
98:JSmol
484:stub
393:TNGU
449:doi
171:EPA
144:CID
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43:H
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