Acephenanthrylene

Acephenanthrylene
Names
	IUPAC name Acephenanthrylene
	Other names 4,5-Benzoacenaphthylene; Benz(e)acenaphthylene; Benzoacenaphthylene
Identifiers
CAS Number	201-06-9;
3D model ( JSmol)	Interactive image;
Beilstein Reference	2247468
ChEBI	CHEBI:33085;
ChemSpider	8789;
PubChem CID	9143;
UNII	FBV4SGU2RK;
CompTox Dashboard (EPA)	DTXSID8075045 ;
	InChI InChI=1S/C16H10/c1-2-6-14-12(4-1)10-13-9-8-11-5-3-7-15(14)16(11)13/h1-10H Key: SQFPKRNUGBRTAR-UHFFFAOYSA-N;
	SMILES C1=CC=C2C(=C1)C=C3C=CC4=C3C2=CC=C4;
Properties
Chemical formula	C16H10
Molar mass	202.256 g·mol−1
Related compounds
Related compounds	Acenaphthylene
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Acephenanthrylene is a tetracyclic polycyclic aromatic hydrocarbon.^[1]

Properties and occurrence

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

Acephenanthrylene has been prepared in 4 steps starting with cyclization of 4-(5-acenapthenyl)butyric acid.^[3]

References

^ "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.
doi:10.1021/jo00350a096
.

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Retrieved from "https://en.wikipedia.org/w/index.php?title=Acephenanthrylene&oldid=1216238931"

[pubchem-1] "Acephenanthrylene". PubChem.

[2] 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.

[3] :10.1021/jo00350a096
.

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