Acephenanthrylene is a tetracyclic polycyclic aromatic hydrocarbon.[1]
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IUPAC name
Acephenanthrylene
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Other names
4,5-Benzoacenaphthylene
Benz(e)acenaphthylene Benzoacenaphthylene | |
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3D model (JSmol)
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2247468 | |
ChEBI | |
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PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C16H10 | |
Molar mass | 202.256 g·mol−1 |
Related compounds | |
Related compounds
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Acenaphthylene |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Properties and occurrence edit
Acephenanthrylene is one of the polycyclic aromatic hydrocarbons formed in combustion of various fuels. However, it is not present as an atmospheric pollutant because its vinylic bridge makes it susceptible to photolytic oxidation once released into the atmosphere.[2]
Preparation edit
Acephenanthrylene has been prepared in 4 steps starting with cyclization of 4-(5-acenapthenyl)butyric acid.[3]
References edit
- ^ "Acephenanthrylene". PubChem.
- ^ National Research Council (US) Committee on Pyrene and Selected Analogues (1983). "3, Atmospheric Transformations of Polycyclic Aromatic Hydrocarbons". Polycyclic Aromatic Hydrocarbons: Evaluation of Sources and Effects. National Academies Press.
- ^ Scott, Lawrence T.; Reinhardt, Gerd; Roelofs, Nicolas H. (1985). "Acephenanthrylene". The Journal of Organic Chemistry. 50 (26): 5886–5887. doi:10.1021/jo00350a096.