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| Name = Benzo[''a'']fluorene |
| Name = Benzo[''a'']fluorene |
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| ImageFile = |
| ImageFile = Benzo(a)fluorene.png |
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| ImageSize = 200px |
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| ImageName = |
| ImageName = Chemical structure of benzo[a]fluorene |
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| IUPACName = 11''H''-Benzo[''a'']fluorene |
| IUPACName = 11''H''-Benzo[''a'']fluorene |
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| OtherNames = 2,3-Benzopyrene |
| OtherNames = 2,3-Benzopyrene |
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Revision as of 13:24, 26 July 2010
![Chemical structure of benzo[a]fluorene](https://thcscience.wiki/term/trichome/?rdp_we_resource=https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FFile%3ABenzo%28a%29fluorene.png)
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| Names | |
|---|---|
| IUPAC name
11H-Benzo[a]fluorene
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| Other names
2,3-Benzopyrene
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| Identifiers | |
| ECHA InfoCard | 100.005.405 |
CompTox Dashboard (EPA)
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| Properties | |
| C17H12 | |
| Molar mass | 216.277 g/mol |
| Density | 0.819 g/cm3 |
| Melting point | 189.5°C |
| Boiling point | 405°C |
| 0.000045 g/L | |
| Solubility | soluble in diethyl ether, benzene, chloroform |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Benzo[a]fluorene (IUPAC name, 11H-Benzo[a]fluorene) is a polycyclic aromatic hydrocarbon (PAH). It is currently listed as a Group 3 carcinogen by the IARC.[2]
References
- ^ Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.), Boca Raton, FL: CRC Press, pp. 3–42, 8–119, ISBN 0849305942
- ^ "Benzo(a)fluorene (IARC Summary & Evaluation, Volume 32, 1983)". IARC. 17 April 1998. Retrieved 22 July 2010.