| Weight | 152.196 g/mol |
|---|---|
| Formula | C12H8 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 0 |
ACENAPHTHYLENE (208-96-8, 34493-60-2)
acenaphthylene, radical ion (1-)
Score:
#508 in Physics
,
#1485 in Chemistry
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- A triruthenium carbonyl cluster bearing a bridging acenaphthylene ligand: an efficient catalyst for reduction of esters, carboxylic acids, and amides by trialkylsilanes. (Journal of Organic Chemistry, 2002)
- Piperonyl butoxide and acenaphthylene induce cytochrome P450 1A2 and 1B1 mRNA in aromatic hydrocarbon-responsive receptor knock-out mouse liver. (Molecular Pharmacology, 1996)
- Kinetics of the reactions of acenaphthene and acenaphthylene and structurally-related aromatic compounds with OH and NO3 radicals, N2O5 and O3 at 296 2 K (International Journal of Chemical Kinetics, 1988)
- Bacterial oxidation of the polycyclic aromatic hydrocarbons acenaphthene and acenaphthylene. (Applied and Environmental Microbiology, 1984)
- X-ray studies on the carbonization and graphitization of acenaphthylene and bifluorenyl (Carbon, 1964)
- Stoichiometric and Catalytic Activation of SiH Bonds by a Triruthenium Carbonyl Cluster, (3,2:3:5-acenaphthylene)Ru3(CO)7: Isolation of the Oxidative Adducts, Catalytic Hydrosilylation of Aldehydes, Ketones, and Acetals, and Catalytic Polymerization of Cyclic Ethers (Organometallics, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H372: Causes damage to organs through prolonged or repeated exposure
Danger Specific target organ toxicity, repeated exposure - Category 1 - H410: Very toxic to aquatic life with long lasting effects
Warning Hazardous to the aquatic environment, long-term hazard - Category 1 - acenaphthylene, radical ion (1-)
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SMILESC1=CC2=C3C(=C1)C=CC3=CC=C2
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InChIKeyHXGDTGSAIMULJN-UHFFFAOYSA-N
- Pubchem - ACENAPHTHYLENE
- Wikipedia - acenaphthylene
Acenaphthylene is a polycyclic aromatic hydrocarbon. The molecule resembles naphthalene with positions 1 and 8 connected by a C2H2 unit. It is a yellow solid.
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