(organic chemistry) C6H10 A compound that occurs in coal tar; a liquid that is used as an alkylation component; used in the manufacture of hexahydrobenzoic acid, adipic acid, and maleic acid.
| Sci-Tech Dictionary: cyclohexene |
(organic chemistry) C6H10 A compound that occurs in coal tar; a liquid that is used as an alkylation component; used in the manufacture of hexahydrobenzoic acid, adipic acid, and maleic acid.
| 5min Related Video: Cyclohexene |
| Wikipedia: Cyclohexene |
| Cyclohexene | |
|---|---|
| IUPAC name |
Cyclohexene
|
| Other names | Tetrahydrobenzene, 1,2,3,4-Tetrahydrobenzene, Benzenetetrahydride, Cyclohex-1-ene, Hexanaphthylene, UN 2256 |
| Identifiers | |
| CAS number | 110-83-8 |
| PubChem | 8079 |
| EC number | 203-807-8 |
| ChEBI | 36404 |
| RTECS number | GW2500000 |
| SMILES |
C1C=CCCC1
|
| InChI |
1/C6H10/c1-2-4-6-5-3-1/h1-2H,3-6H2
|
| Properties | |
| Molecular formula | C6H10 |
| Molar mass | 82.143 g/mol |
| Appearance | Liquid |
| Density | 0.8110 g/cm3 |
| Melting point |
-103.5 °C |
| Boiling point |
82.98 °C |
| Solubility in water | 250 mg/l |
| Vapor pressure | 8.93 kPa (20 °C)
11.9 kPa (25 °C) |
| Hazards | |
| R-phrases | R11, R19, R21/22 |
| S-phrases | S16, S23, S24, S25, S33 |
| NFPA 704 | |
| Flash point | -12 °C (10 °F) c.c. |
| Autoignition temperature |
244 °C (471.2 °F) |
| Explosive limits | 1 - 5 % |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
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| Infobox references | |
Cyclohexene is a hydrocarbon with the formula C6H10. This cycloalkene is a colorless liquid with a sharp smell. It is an intermediate in various industrial processes. Cyclohexene is not very stable upon long term storage with exposure to light and air because it forms peroxides.
Contents |
Cyclohexene is produced by the partial hydrogenation of benzene, a process developed by Asahi Chemical Company. It is converted to cyclohexanol, which is dehydrogenated to give cyclohexanone, a precursor to caprolactam.[1] Cyclohexene is also a precursor to adipic acid, maleic acid, dicyclohexyladipate, and cyclohexeneoxide. Furthermore, it is used as a solvent.
A common experiment for beginning organic chemistry students is the acid catalyzed dehydration of cyclohexanol with distillative removal of the resulting cyclohexene from the reaction mixture:
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