Acenaphthene
From Wikipedia, the free encyclopedia
| Acenaphthene | |
|---|---|
| Image:Acenaphthene.png | |
| General | |
| Systematic name | 1,8-dihydroacenaphthalene |
| Other names | 1,8-ethylenenaphthalene, peri-ethylenenaphthalene, naphthyleneethylene |
| Molecular formula | C12H10 |
| SMILES | c1cc2cccc3CCc(c1)c23 |
| Molar mass | 154.21 g/mol |
| Appearance | white or pale yellow crystalline powder |
| CAS number | [83-32-9] |
| Properties | |
| Density and phase | 1.02 g/cm³ |
| Solubility in water | Insoluble |
| Melting point | 93-95 °C |
| Boiling point | 280 °C |
| Structure | |
| Crystal structure | ? |
| Dipole moment | ? D |
| Hazards | |
| MSDS | External MSDS |
| Main hazards | ? |
| NFPA 704 | |
| Flash point | ?°C |
| R/S statement | R: R36 R37 R38 S: S26 S36 |
| RTECS number | ? |
| Supplementary data page | |
| Structure and properties | n, εr, etc. |
| Thermodynamic data | Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| Related compounds | |
| Related compounds | acenaphthylene |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Acenaphthene is a polycyclic aromatic hydrocarbon consisting of naphthalene with an ethylene bridge connecting positions 1 and 8. An alternative name, 1,2 dihydroacenaphthylene, emphasizes that it is a hydrogenated form of acenaphthylene. It is a constituent of coal tar.
It does not appear to be carcinogenic.

