Structure via PubChem · Public domain (PubChem)
acenaphthenequinone
Sign in to saveAlso known as 1,2-acenaphthenequinone, 1,2-acenaphthenedione, 1,2-acenaphthylenedione, acenaphthylene-1,2-quinone, acenaphthylenedione, acenaphthodione, diketoacenaphthene, Aq
Acenaphthoquinone is a quinone derived from acenaphthene. It is a water-insoluble yellow solid. It is a precursor to some agrichemicals and dyes.
In the Vinony graph
Vinony's link graph records 3 inbound references to acenaphthenequinone, and connects out to International Standard Book Number, digital object identifier and chemical formula.
Vinony files it under Chembox having GHS data, Chembox image size set and ECHA InfoCard ID from Wikidata.
Vinony links it to 16 Wikipedia language editions.
Chemical data
- Formula
- C12H6O2
- Molecular weight
- 182.17 g/mol
- IUPAC name
- acenaphthylene-1,2-dione
- SMILES
- C1=CC2=C3C(=C1)C(=O)C(=O)C3=CC=C2
- InChIKey
- AFPRJLBZLPBTPZ-UHFFFAOYSA-N
- XLogP
- 1.9
- Polar surface area
- 34.1 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Mass
- 182.037
Show 4 more facts
- chemical formula
- C₁₂H₆O₂
- canonical SMILES
- C1=CC2=C3C(=C1)C(=O)C(=O)C3=CC=C2
- melting point
- 258
- Commons category
- Acenaphthoquinone
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Preparation
- References
- External links
Acenaphthoquinone is a quinone derived from acenaphthene. It is a water-insoluble yellow solid. It is a precursor to some agrichemicals and dyes.
==Preparation== The compound is prepared in the laboratory by oxidation of acenaphthene with potassium dichromate. Commercially, oxidation is effected with peroxide. Over-oxidation gives naphthalenedicarboxylic anhydride.
Excerpted from Wikipedia’s “acenaphthenequinone” article, available under the CC BY-SA 4.0 licence.
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