2-Ethylanthraquinone: Difference between revisions
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Script assisted update of identifiers from ChemSpider, CommonChemistry and FDA for the Chem/Drugbox validation project - Updated: InChI1->InChI StdInChI StdInChIKey. |
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| verifiedrevid = 399296420 |
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| Name = 2-Ethylanthraquinone |
| Name = 2-Ethylanthraquinone |
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| ImageFile = 2-Ethylanthraquinone.svg |
| ImageFile = 2-Ethylanthraquinone.svg |
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| OtherNames = 2-Ethyl-9,10-anthracenedione |
| OtherNames = 2-Ethyl-9,10-anthracenedione |
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| Section1 = {{Chembox Identifiers |
| Section1 = {{Chembox Identifiers |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID = 6514 |
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| InChI = 1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3 |
| InChI = 1/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3 |
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| InChIKey = SJEBAWHUJDUKQK-UHFFFAOYAW |
| InChIKey = SJEBAWHUJDUKQK-UHFFFAOYAW |
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| SMILES = O=C2c1c(cccc1)C(=O)c3c2ccc(c3)CC |
| SMILES = O=C2c1c(cccc1)C(=O)c3c2ccc(c3)CC |
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| StdInChI_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChI = 1S/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3 |
| StdInChI = 1S/C16H12O2/c1-2-10-7-8-13-14(9-10)16(18)12-6-4-3-5-11(12)15(13)17/h3-9H,2H2,1H3 |
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| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} |
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| StdInChIKey = SJEBAWHUJDUKQK-UHFFFAOYSA-N |
| StdInChIKey = SJEBAWHUJDUKQK-UHFFFAOYSA-N |
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| CASNo = 84-51-5 |
| CASNo = 84-51-5 |
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Revision as of 09:40, 28 November 2010
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| Names | |
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| Other names
2-Ethyl-9,10-anthracenedione
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.001.396 |
| EC Number |
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CompTox Dashboard (EPA)
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| Properties | |
| C16H12O2 | |
| Molar mass | 236.27 g/mol |
| Density | 650 kg·m−3 |
| Melting point | 105 °C (221 °F; 378 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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2-Ethylanthraquinone is an aromatic organic compound closely related to anthracene.
It is commonly used along with 2-ethyl-9,10-dihydroxyanthracene to create hydrogen peroxide (H2O2) by the Riedl-Pfleiderer, or autoxidation, process:
 | This article about an aromatic compound is a stub. You can help Wikipedia by expanding it. |