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Cyclohexene

 
Sci-Tech Dictionary: cyclohexene
(¦sī·klō′hek′sēn)

(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.


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Wikipedia: Cyclohexene
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Cyclohexene
Cyclohexene.png
Cyclohexene-conformation-2D-skeletal.png
IUPAC name
Other names Tetrahydrobenzene, 1,2,3,4-Tetrahydrobenzene, Benzenetetrahydride, Cyclohex-1-ene, Hexanaphthylene, UN 2256
Identifiers
CAS number 110-83-8 Yes check.svgY
PubChem 8079
EC number 203-807-8
ChEBI 36404
RTECS number GW2500000
SMILES
InChI
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
NFPA 704.svg
3
1
0
 
Flash point -12 °C (10 °F) c.c.
Autoignition
temperature
244 °C (471.2 °F)
Explosive limits 1 - 5 %
 Yes check.svgY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
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

Production and uses

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.

Laboratory experiments

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:

Cyclohexensynthese1.svg
Cyclohexensynthese2.svg
  • Refractive Index: 1.4465
  • Critical temperature: 287.2 °C (560.4 K)

See also

References

  1. ^ Michael T. Musser "Cyclohexanol and Cyclohexanone" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005.doi:10.1002/14356007.a08_217

External links


 
 

 

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Sci-Tech Dictionary. McGraw-Hill Dictionary of Scientific and Technical Terms. Copyright © 2003, 1994, 1989, 1984, 1978, 1976, 1974 by McGraw-Hill Companies, Inc. All rights reserved.  Read more
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