Cyclohexane, (1-methylethylidene)-

• Formula: C₉H₁₆
• Molecular weight: 124.2233
• IUPAC Standard InChI: InChI=1S/C9H16/c1-8(2)9-6-4-3-5-7-9/h3-7H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: CUYJYVAWBJXBIC-UHFFFAOYSA-N Copy
• CAS Registry Number: 5749-72-4
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Cyclohexane, isopropylidene-; Isopropylidenecyclohexane
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• Information on this page:
  • Phase change data
  • Reaction thermochemistry data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Phase change data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

Reaction thermochemistry data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

Note: Please consider using the reaction search for this species. This page allows searching of all reactions involving this species. A general reaction search form is also available. Future versions of this site may rely on reaction search pages in place of the enumerated reaction displays seen below.

Individual Reactions

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By formula: C₉H₁₆ = C₉H₁₆

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Gold, 1970
Gold, P.I., The Kinetics of Acid-catalysed Equilibrations of Endo- and Exo-cyclic Olefins, J. Chem. Soc. B, 1970, 1970, 1761-6. [all data]

Chiurdoglu, Laune, et al., 1956
Chiurdoglu, G.; Laune, J.; Poelmans, M., Acyclic compounds with Quarternary Carbon IV. Conjugation with 1-Ethoxycaronylcycloprpanesprirocyclanes, Bull Soc. Chim. Belges, 1956, 65, 257-69. [all data]

Von Auwers and Ellinger, 1912
Von Auwers, K.; Ellinger, P., Justus Liebigs Ann. Chem., 1912, 387, 200-39. [all data]

Wallach and Mallison, 1908
Wallach, O.; Mallison, H., Knowledge of Terpenes and Essential Oils. VII. Condensation of Cyclohexanone with Bromobutyric Acid Ester, Justus Liebigs Ann. Chem., 1908, 360, 68-70. [all data]

Wallach, 1908
Wallach, O., Knowledge of Terpenes and Essential Oils, Justus Liebigs Ann. Chem., 1908, 360, 26-44. [all data]

Bigley and May, 1970
Bigley, D.B.; May, R.W., The kinetics of acid-catalysed equilibrations of endo- and exo-cyclic olefins, J. Chem. Soc. B, 1970, 1761-1766. [all data]

Notes

Go To: Top, Phase change data, Reaction thermochemistry data, References

• Symbols used in this document:
  

  Tboil	Boiling point
  ΔrH°	Enthalpy of reaction at standard conditions

• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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