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acenaphthenequinone

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EntityQ2739953· pop 17· linked from 3 articles

acenaphthenequinone

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Also 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.

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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

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Encyclopedic overview

3 sections
Contents
  • 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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