1-Phenylcyclohexanol

• Formula: C₁₂H₁₆O
• Molecular weight: 176.2548
• IUPAC Standard InChI: InChI=1S/C12H16O/c13-12(9-5-2-6-10-12)11-7-3-1-4-8-11/h1,3-4,7-8,13H,2,5-6,9-10H2 Copy

  
• IUPAC Standard InChIKey: DTTDXHDYTWQDCS-UHFFFAOYSA-N Copy
• CAS Registry Number: 1589-60-2
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Other names: Cyclohexanol, 1-phenyl-; 1-Phenyl-1-cyclohexanol; 1-Phenylcyclohexanol-1; Benzene, cyclohex-1-yl-1-ol-
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• Information on this page:
  • Phase change data
  • Gas phase ion energetics data
  • IR Spectrum
  • UV/Visible spectrum
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
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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

Gas phase ion energetics 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: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

Appearance energy determinations

IR Spectrum

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Gas Phase Spectrum

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Additional Data

UV/Visible spectrum

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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: Victor Talrose, Eugeny B. Stern, Antonina A. Goncharova, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina

Spectrum

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Additional Data

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.

Nenitzescu and Necsoiu, 1950
Nenitzescu, C.D.; Necsoiu, I., The Synthesis of Cyclic Alcohols nd Olefins by the Interaction of Dimagnesium Halides and Esters, J. Am. Chem. Soc., 1950, 72, 3483. [all data]

Signaigo and Cramer, 1933
Signaigo, F.K.; Cramer, P.L., The preparation of some mono- and dialkylcylohexanes, J. Am. Chem. Soc., 1933, 55, 3326-32. [all data]

Mikaya, Zaikin, et al., 1979
Mikaya, A.I.; Zaikin, V.G.; Finkel'stein, E.S.; Vdovin, V.M., Mass-spectrometric investigation of aromatic derivatives of cycloalkanes and cycloalkanols, Izv. Akad. Nauk SSSR, Ser. Khim., 1979, 10, 2221. [all data]

Lavruchin, Verkhovod, et al., 1955
Lavruchin, V.F.; Verkhovod, N.N.; Movchan, P.K., Halochromism of tertiary alicyclic and aliphatic carbinols, Dokl. Akad. Nauk SSSR, 1955, 105, 4, 723-726. [all data]

Notes

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• Symbols used in this document:
  

  AE	Appearance energy
  Tfus	Fusion (melting) point

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