“Acenaphthoquinone”的意思、由来-开放百科全书

词条

Acenaphthoquinone

释义

References
External links

{{chembox
| Watchedfields = changed
| verifiedrevid = 477238198
| ImageFile_Ref = {{chemboximage|correct|??}}
| ImageFile = Acenaphthoquinone.png
| ImageSize = 140px
| ImageAlt = Skeletal formula
| ImageFile1 = Acenaphthoquinone-3D-balls.png
| ImageSize1 = 160
| ImageAlt1 = Ball-and-stick model
| PIN = Acenaphthylene-1,2-dione
| OtherNames = Acenaphthoquinone (no longer accepted even in general nomenclature^[1])
Acenaphthenequinone
1,2-Acenaphthenequinone
Acenaphthenedione
1,2-Acenaphthylenedione
Acenaphthene-1,2-dione
1,2-Diketoacenaphthene
|Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 6468
| InChIKey = AFPRJLBZLPBTPZ-UHFFFAOYAC
| ChEMBL_Ref = {{ebicite|correct|EBI}}
| ChEMBL = 395653
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/C12H6O2/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(11)14/h1-6H
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = AFPRJLBZLPBTPZ-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 82-86-0
| EINECS = 201-441-3
| PubChem = 6724
| SMILES = O=C3c2cccc1cccc(c12)C3=O
| InChI = 1/C12H6O2/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(11)14/h1-6H
| ChEBI_Ref = {{ebicite|correct|EBI}}
| ChEBI = 15342
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = C02807
|Section2={{Chembox Properties
| C=12 | H=6 | O=2
| Appearance = Purple-yellow crystals to brown powder
| Density =
| MeltingPtC = 257 to 261
| MeltingPt_notes =
| BoilingPt =
| Solubility = Insoluble (90.1 mg/l)
|Section3={{Chembox Hazards
| MainHazards = Irritating
| FlashPt =
| AutoignitionPt =
| NFPA-H = 2
| NFPA-F = 0
| NFPA-R = 0
| NFPA-S =
| RPhrases = {{R36/37/38}}
| SPhrases = {{S26}}, {{S37/39}}
}}

Acenaphthoquinone is a quinone derived from acenaphthene. It is insoluble in water, but soluble in alcohol. It is used as an intermediate for the manufacturing of dyes, pharmaceuticals and pesticides. It is also used in chemical research as a drug and therapeutic agent.

The substance is classified as an irritant. Its carcinogenic properties have not been fully investigated yet.

References

1. ^{{cite book | title = Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book) | publisher = The Royal Society of Chemistry | date = 2014 | location = Cambridge | page = 724 | doi = 10.1039/9781849733069-FP001 | isbn = 978-0-85404-182-4}}

External links

[https://web.archive.org/web/20060518002254/http://www.npi.gov.au/database/substance-info/profiles/74.html National Pollutant Inventory - Polycyclic Aromatic Hydrocarbon Fact Sheet]
[https://web.archive.org/web/20050414054720/http://wlapwww.gov.bc.ca/wat/wq/BCguidelines/pahs/pahs-01.htm PAHs - including structural diagrams]
[https://archive.is/20121209043934/http://www.chemicalland21.com/arokorhi/specialtychem/finechem/1,2-ACENAPHTHYLENEDIONE.htm Entry at ChemicalLand21.com]
MSDS at chemphys.gcsu.edu{{dead link|date=October 2016 |bot=InternetArchiveBot |fix-attempted=yes }}

2 : Quinones|Polycyclic aromatic compounds

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