This is an old revision of this page, as edited by Beetstra (talk | contribs) at 17:49, 8 August 2011 (Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'DrugBank', 'UNII', 'ChEBI').). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.
Revision as of 17:49, 8 August 2011 by Beetstra (talk | contribs) (Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'DrugBank', 'UNII', 'ChEBI').)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)This article is an orphan, as no other articles link to it. Please introduce links to this page from related articles; try the Find link tool for suggestions. (February 2009) |
Names | |
---|---|
IUPAC name 2,3,5,6-Tetramethyl-1,4-benzoquinone | |
Other names Tetramethyl-p-benzoquinone | |
Identifiers | |
CAS Number | |
3D model (JSmol) | |
ChEBI | |
ChEMBL | |
ChemSpider | |
DrugBank | |
ECHA InfoCard | 100.007.646 |
UNII | |
CompTox Dashboard (EPA) | |
InChI
| |
SMILES
| |
Properties | |
Chemical formula | C10H12O2 |
Molar mass | 164.20408 g/mol |
Melting point | 109 - 114 °C |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is ?) Infobox references |
Duroquinone is a derivative of 1,4-benzoquinone.
It is also used in the formation of a "nano brain" (16 duroquinone molecules surrounding a 17th in the middle).
References
- *Fildes, Jonathan (2008-03-11). "Chemical brain controls nanobots". British Broadcasting Corporation. Retrieved 2008-03-11.
{{cite news}}
: Cite has empty unknown parameter:|coauthors=
(help)
This article about a ketone is a stub. You can help Misplaced Pages by expanding it. |