| Weight | 300.36 g/mol |
|---|---|
| Formula | C24H12 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 7 |
| Rotatable Bonds | 0 |
CORONENE (191-07-1)
Score:
#2076 in Physics
,
#6459 in Chemistry
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- Noncovalent functionalization, exfoliation, and solubilization of graphene in water by employing a fluorescent coronene carboxylate. (Chemistry: A European Journal, 2010)
- Incorporation and Manipulation of Coronene in an Organic Template Structure (Langmuir, 2004)
- CounterRotating Ring Currents in Coronene and Corannulene (Angewandte Chemie, 2001)
- Liquid crystalline coronene derivatives with extraordinary fluorescence properties (Angewandte Chemie, 1998)
- Infrared Spectroscopy of Matrix-Isolated Polycyclic Aromatic Hydrocarbon Cations. 2. The Members of the Thermodynamically Most Favorable Series through Coronene (The Journal of Physical Chemistry, 1995)
- Crystallization of Large Planar Polycyclic Aromatic Hydrocarbons: The Molecular and Crystal Structures of Hexabenzo[bc,ef,hi,kl,no,qr]coronene and Benzo[1,2,3-bc:4,5,6-b'c']dicoronene (Journal of the American Chemical Society, 1995)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC2=C3C4=C1C=CC5=C4C6=C(C=C5)C=CC7=C6C3=C(C=C2)C=C7
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InChIKeyVPUGDVKSAQVFFS-UHFFFAOYSA-N
- Pubchem - CORONENE
- Wikipedia - coronene
Coronene (also known as superbenzene) is a polycyclic aromatic hydrocarbon (PAH) comprising six peri-fused benzene rings. Its chemical formula is C 24H 12. It is a yellow material that dissolves in common solvents including benzene, toluene, and dichloromethane.
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