Indenone

Indenone
Names
	Preferred IUPAC name 1H-Inden-1-one
Identifiers
CAS Number	480-90-0;
3D model (JSmol)	Interactive image;
ChemSpider	9990041;
PubChem CID	11815384;
UNII	B65N387LDP ;
CompTox Dashboard (EPA)	DTXSID80473374 ;
	InChI InChI=1S/C9H6O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-6H Key: SNWQUNCRDLUDEX-UHFFFAOYSA-N;
	SMILES c1ccc2c(c1)C=CC2=O;
Properties
Chemical formula	C9H6O
Molar mass	130.146 g·mol−1
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H315, H319, H335
Precautionary statements	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Indenone is a polycyclic ketone with chemical formula C₉H₆O. It is composed of a benzene ring fused with a cyclopentenone ring. Indenones can be used as intermediates in the synthesis of more complex molecules.^[1]

References

^ Larock, R. C.; M. J. Doty; S. Cacchi (1993). "Synthesis of indenones via palladium-catalyzed annulation of internal alkynes". J. Am. Chem. Soc. 58 (17): 4579–4583. doi:10.1021/jo00069a017.

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[1] Larock, R. C.; M. J. Doty; S. Cacchi (1993). "Synthesis of indenones via palladium-catalyzed annulation of internal alkynes". J. Am. Chem. Soc. 58 (17): 4579–4583. doi:10.1021/jo00069a017.

[1]

Indenone

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Indenone

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