Bindone: Difference between revisions

Bindone
Names
	IUPAC name 2-(3-oxoinden-1-ylidene)indene-1,3-dione
Identifiers
CAS Number	1707-95-5;
3D model (JSmol)	Interactive image;
ChemSpider	14812;
ECHA InfoCard	100.015.415
EC Number	216-956-9;
PubChem CID	15569;
UNII	INB7800050;
CompTox Dashboard (EPA)	DTXSID00168932 ;
	InChI InChI=1S/C18H10O3/c19-15-9-14(10-5-1-2-6-11(10)15)16-17(20)12-7-3-4-8-13(12)18(16)21/h1-8H,9H2 Key: YMFDOLAAUHRURP-UHFFFAOYSA-N;
	SMILES C1C(=C2C(=O)C3=CC=CC=C3C2=O)C4=CC=CC=C4C1=O;
Properties
Chemical formula	C18H10O3
Molar mass	274.275 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

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Revision as of 08:07, 19 July 2018

Bindone is an aromatic triketone. It is a condensation product of 1,3-indandione. Bindone is used as a colour test when detecting primary amines.^[1]

Bindone formation from two molecules of 1,3-indandione

References

^ Vecera, Miroslov (2012). Detection and Identification of Organic Compounds. Springer Science & Business Media. p. 319. ISBN 9781468418330.

[1] Vecera, Miroslov (2012). Detection and Identification of Organic Compounds. Springer Science & Business Media. p. 319. ISBN 9781468418330.

[1]

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-'''Bindone''' is an aromatic triketone. It is a condensation product of [[1,3-indandione]].
+'''Bindone''' is an aromatic triketone. It is a condensation product of [[1,3-indandione]]. Bindone is used as a colour test when detecting [[primary amine]]s.<ref>{{cite book |last1=Vecera |first1=Miroslov |title=Detection and Identification of Organic Compounds |date=2012 |publisher=Springer Science & Business Media |isbn=9781468418330 |page=319 |url=https://books.google.com/books?id=RabhBwAAQBAJ&pg=PA319 |language=en}}</ref>
 [[File:Bindone-formation.svg|thumb|Bindone formation from two molecules of 1,3-indandione]]