1-Fluoronaphthalene
Names | |
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Preferred IUPAC name
1-Fluoronaphthalene | |
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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UNII | |
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: | |
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
[edit]1-Fluoronaphthalene can be obtained by reacting naphthalene with Selectfluor.[2]
Properties
[edit]1-Fluoronaphthalene is a colorless, combustible liquid, which is insoluble in water.[3]
Applications
[edit]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.
1-Fluoronaphthalene is also used as a component of the Organic Check Material mounted in canisters on Mars Science Laboratory Curiosity rover. It's used for calibrating the Sample Analysis at Mars (SAM) instrument suite, being a synthetic organic compound not found in nature on Earth and not expected on Mars.[4]
See also
[edit]References
[edit]- ^ "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.
- ^ "Sampling System". Jet Propulsion Laboratory. msl-scicorner.jpl.nasa.gov. Archived from the original on 20 March 2009. Retrieved 28 July 2019.