| Weight | 182.178 g/mol |
|---|---|
| Formula | C12H6O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 0 |
Acenaphthenequinone (82-86-0)
Score:
#5470 in Chemistry
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- Acenaphthenequinone thiosemicarbazone and its transition metal complexes: Synthesis, structure, and biological activity (Journal of Inorganic Biochemistry, 1997)
- An environmental quinoid polycyclic aromatic hydrocarbon, acenaphthenequinone, modulates cyclooxygenase-2 expression through reactive oxygen species generation and nuclear factor kappa B activation in A549 cells. (Toxicological Sciences, 2007)
- General non-catalytic approach to spiroacenaphthylene heterocycles: multicomponent assembling of acenaphthenequinone, cyclic CH-acids and malononitrile (Tetrahedron, 2012)
- The n * Transition Band of Acenaphthenequinone (Bulletin of the Chemical Society of Japan, 1960)
- Communications- A New Carbon-Carbon Condensation Reaction Induced by Phosphite Esters. Formation of a 2:1 Adduct in the Reduction of Acenaphthenequinone with Trimethyl Phosphite (Journal of Organic Chemistry, 1961)
- Superacid-catalyzed polycondensation of acenaphthenequinone with aromatic hydrocarbons (Macromolecules, 2005)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C3C(=C1)C(=O)C(=O)C3=CC=C2
-
InChIKeyAFPRJLBZLPBTPZ-UHFFFAOYSA-N
- Pubchem - Acenaphthenequinone
- Wikipedia - acenaphthenequinone
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.
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Acenaphthenequinone
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