Structure via PubChem · Public domain (PubChem)
cyclohexene
Sign in to saveAlso known as Benzene tetrahydride, Tetrahydrobenzene, benzenetetrahydride, 3,4,5,6-tetrahydrobenzene, 1,2,3,4-tetrahydrobenzene, Zyklohexen, 1-cyclohexene, cyclohex-1-ene
Cyclohexene is a hydrocarbon with the formula . It is a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon.
Chemical data
- Formula
- C6H10
- Molecular weight
- 82.14 g/mol
- IUPAC name
- cyclohexene
- SMILES
- C1CCC=CC1
- InChIKey
- HGCIXCUEYOPUTN-UHFFFAOYSA-N
- XLogP
- 2.9
- Polar surface area
- 0 Ų
- H-bond donors
- 0
- H-bond acceptors
- 0
- Formal charge
- 0
via PubChem
Wikidata facts
- Mass
- 82.078
Show 13 more facts
- chemical formula
- C₆H₁₀
- vapor pressure
- 67
- canonical SMILES
- C1CCC=CC1
- flash point
- 11
- NIOSH Pocket Guide ID
- 0167
- density
- 0.81
- Commons category
- Cyclohexene
- immediately dangerous to life or health
- 6720
- melting point
- -103.5
- boiling point
- 82.98
- ionization energy
- 8.95
- time-weighted average exposure limit
- 1015
- electric dipole moment
- 0.332
via Wikidata · CC0
~2 min read
Article
6 sectionsContents
- Production and uses
- Reactions and uses
- Structure
- See also
- References
- External links
Cyclohexene is a hydrocarbon with the formula . It is a cycloalkene. At room temperature, cyclohexene is a colorless liquid with a sharp odor. Among its uses, it is an intermediate in the commercial synthesis of nylon.
==Production and uses== Cyclohexene is produced by the partial hydrogenation of benzene, a process developed by the Asahi Chemical company. The main product of the process is cyclohexane because cyclohexene is more easily hydrogenated than benzene.