1-Fluoronaphthalene
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| Names | |
|---|---|
| Other names
α-fluoronaphthalene
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.005.717 |
| EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C 10H 7F | |
| Appearance | Colorless liquid |
| Melting point | −13 °C (9 °F; 260 K) |
| Boiling point | 215 °C (419 °F; 488 K) |
| insoluble | |
| Hazards | |
| GHS labelling: | |
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| Warning | |
| Flash point | 65 °C (149 °F; 338 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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1-Fluornaphthalene is an organofluorine chemical compound from the group of naphthalene derivatives and fluoroaromatics. Its chemical formula is C
10H
7F.[1]
Synthesis
1-Fluoronaphthalene can be obtained by reacting naphthalene with Selectfluor.[2]
Properties
1-Fluornaphthalene is a colorless, combustible liquid, which is insoluble in water.[3]
Applications
1-Fluoronaphthalene was used for the tert-butyllithium-mediated synthesis of 6-substituted phenanthridines. It has also been used in the synthesis of LY248686, a potent inhibitor of serotonin and norepinephrine uptake.
See also
References
- ^ "1-Fluoronaphthalene". Sigma Aldrich. sigmaaldrich.com. Retrieved 13 June 2017.
- ^ Atta-Ur-Rahman (2006). Advances in Organic Synthesis: Modern Organofluorine Chemistry-Synthetic Aspects. Bentham Science Publishers. p. 246. ISBN 1-60805-198-6.
- ^ "1-FLUORONAPHTHALENE". CAMEO Chemicals. cameochemicals.noaa.gov. Retrieved 13 June 2017.