Misplaced Pages

HHTDD: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively← Previous editNext edit →Content deleted Content addedVisualWikitext
Revision as of 11:54, 5 September 2011 editZéroBot (talk | contribs)704,777 editsm r2.7.1) (robot Adding: zh:六硝基六氮杂三环十二烷二酮← Previous edit Revision as of 12:04, 5 September 2011 edit undoCheMoBot (talk | contribs)Bots141,565 edits Updating {{chembox}} (no changed fields - added verified revid - updated 'DrugBank_Ref', 'UNII_Ref', 'ChEMBL_Ref', 'ChEBI_Ref', 'KEGG_Ref', 'ChEBI_Ref') per Chem/Drugbox validation (report [[Wikipedia_talk:WikiProject_Chemicals|errorNext edit →
Line 1: Line 1:
{{Chembox {{Chembox
| verifiedrevid = 399424770 | verifiedrevid = 438286974
| ImageFile = HHTDD_structure.png | ImageFile = HHTDD_structure.png
| ImageSize = 150px | ImageSize = 150px

Revision as of 12:04, 5 September 2011

HHTDD
Names
IUPAC name 2,6-dioxo-1,3,4,5,7,8-hexanitrodecahydro-1H,5H-diimidazopyrazine
Identifiers
3D model (JSmol)
ChemSpider
CompTox Dashboard (EPA)
InChI
  • 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/h1-4HKey: ZFBXJPJQJKATGM-UHFFFAOYSA-N
  • 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/h1-4HKey: ZFBXJPJQJKATGM-UHFFFAOYAE
SMILES
  • O=C2N((=O)=O)C3C(N2(=O)=O)N((=O)=O)C1C(N3(=O)=O)N((=O)=O)C(=O)N1(=O)=O
Properties
Chemical formula C6H4N12O14
Molar mass 468.168
Explosive data
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

HHTDD is a powerful but moisture sensitive explosive compound. It is essentially an open analogue of the cyclic nitroamine cage compounds such as CL-20. While it is highly explosive, with a velocity of detonation 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.

See also

References

  1. 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". The Journal of Organic Chemistry. 56 (10): 3413–3419. doi:10.1021/jo00010a043.


Stub icon

This explosives-related article is a stub. You can help Misplaced Pages by expanding it.

Categories: