Indenone
Names | |
---|---|
Preferred IUPAC name 1H-Inden-1-one | |
Identifiers | |
CAS Number |
|
3D model (JSmol) |
|
ChemSpider |
|
PubChem CID |
|
UNII |
|
CompTox Dashboard (EPA) |
|
InChI
| |
| |
Properties | |
Chemical formula | C9H6O |
Molar mass | 130.146 g·mol−1 |
Hazards | |
GHS labelling: | |
Pictograms | |
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 |
Chemical compound
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]
See also
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.
- v
- t
- e