1,4-Diamino-2,3-dihydroanthraquinone: Difference between revisions

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	== reactions ==		== reactions ==
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	==References==		==References==
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	1. ^ Heyer, Thomas; Hans-Joachim Niclas, Stephan Dietzel (2010).		1. ^ Heyer, Thomas; Hans-Joachim Niclas, Stephan Dietzel (2010).
	"NMR-Untersuchungen zur Tautomerie bei Dihydroanthracendionen".		"NMR-Untersuchungen zur Tautomerie bei Dihydroanthracendionen".
	Zeitschrift für Chemie 29 (4): 139–140. doi:10.1002/zfch.19890290408. ISSN 00442402.		Zeitschrift für Chemie 29 (4): 139–140. doi:10.1002/zfch.19890290408. ISSN 00442402.


	{{DEFAULTSORT:Diamino-2,3-dihydroanthraquinone, 1,4-}}		{{DEFAULTSORT:Diamino-2,3-dihydroanthraquinone, 1,4-}}
⚫	{{organic-compound-stub}}

	]		]


		⚫	{{organic-compound-stub}}

Revision as of 18:04, 28 February 2011

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1,4-Diamino-2,3-dihydroanthraquinone
Names

IUPAC name 1,4-Diaminoanthracene-9,10-dione
Other names Solvent violet 47
Identifiers
CAS Number	81-63-0
3D model (JSmol)	Interactive image
ChemSpider	4511053
ECHA InfoCard	100.001.244
PubChem CID	5354979
CompTox Dashboard (EPA)	DTXSID70883261
InChI InChI=1S/C14H12N2O2/c15-9-5-6-10(16)12-11(9)13(17)7-3-1-2-4-8(7)14(12)18/h1-4H,5-6,15-16H2Key: SSGALQHXKMAJTL-UHFFFAOYSA-N
SMILES O=C/2c1ccccc1C(=O)C=3/C\2=C(/N)CCC=3N
Properties
Chemical formula	C₁₄H₁₂N₂O₂
Molar mass	240.262 g·mol
Appearance	Dark greenish to brownish powder
Density	1.4 g/cm
Boiling point	375.1 °C (707.2 °F; 648.2 K)
Solubility in water	Soluble in hot nitrobenzene
Hazards
Occupational safety and health (OHS/OSH):
Main hazards	Mutagenic; emits NO_x vapors when heated to decomposition.
Flash point	180.7 °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

Chemical compound

1,4-Diamino-2,3-dihydroanthraquinone is an anthraquinone dye used with Disperse Red 9 in colored smoke to introduce a violet color. It is also used in dyes and marine flares.

1,4-Diamino-anthraquinone is reacted With sodium dithionite

This section is empty. You can help by adding to it. (February 2011)

  1. ^ Heyer, Thomas; Hans-Joachim Niclas, Stephan Dietzel (2010).

"NMR-Untersuchungen zur Tautomerie bei Dihydroanthracendionen".

Zeitschrift für Chemie 29 (4): 139–140. doi:10.1002/zfch.19890290408. ISSN 00442402.

This article about an organic compound is a stub. You can help Misplaced Pages by expanding it.