// Workers AI · dad joke modeWhat did hydrindane say to its date? You're a ring above the rest.
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| Names | |
|---|---|
| IUPAC name
2,3,3a,4,5,6,7,7a-octahydro-1H-indene | |
| Other names
octahydroindene, hexahydroindane, bicyclo[4.3.0]nonane | |
| Identifiers | |
3D model (JSmol) |
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| 2321743 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.007.104 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C9H16 | |
| Molar mass | 124.227 g·mol−1 |
| Density | 0.90732 g/cm3 |
| Melting point | −53 °C (−63 °F; 220 K) |
| Boiling point | 165.5–167.5 °C (329.9–333.5 °F; 438.6–440.6 K) |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| H226, H302, H413 | |
| P210, P233, P240, P241, P242, P243, P264, P270, P273, P280, P301+P317, P303+P361+P353, P330, P370+P378, P403+P235, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Hydrindane is an organic compound with the formula C9H16. A bicyclic molecule, it is the hydrogenated derivative of the more common hydrocarbons indane and indene. Isomers of hydrindane include the compound with cis-fused rings and the chiral trans-fused derivative.[1]
Occurrence
[edit]
Hydrindane is a component of diesel fuels produced by hydrocracking.[2] Hydrindane is a subunit of many steroids.[3]
References
[edit]- ↑ Norman L. Allinger, James L. Coke (1960), "The Relative Stabilities of cis and trans Isomers. VII. The Hydrindanes 1,2", Journal of the American Chemical Society, vol. 82, no. 10, pp. 2553–2556, Bibcode:1960JAChS..82.2553A, doi:10.1021/ja01495a039
- ↑ McVicker, G. (2002). "Selective Ring Opening of Naphthenic Molecules". Journal of Catalysis. 210 (1): 137–148. Bibcode:2002JCat..210..137M. doi:10.1006/jcat.2002.3685.
- ↑ Hans Beyer, Wolfgang Walter (1978), Lehrbuch der organischen Chemie (18. ed.), Stuttgart: S. Hirzel Verlag, p. 350, ISBN 3-7776-0342-2