Phenol, 2-ethenyl-

• Formula: C₈H₈O
• Molecular weight: 120.1485
• IUPAC Standard InChI: InChI=1S/C8H8O/c1-2-7-5-3-4-6-8(7)9/h2-6,9H,1H2 Copy

  
• IUPAC Standard InChIKey: JESXATFQYMPTNL-UHFFFAOYSA-N Copy
• CAS Registry Number: 695-84-1
• Chemical structure:
  This structure is also available as a 2d Mol file
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• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
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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 Chromatography

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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

Van Den Dool and Kratz RI, non-polar column, custom temperature program

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Van Den Dool and Kratz RI, polar column, custom temperature program

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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.

Dale and Hennis, 1958
Dale, W.J.; Hennis, H.E., Substituted Styrenes III.. The Synthesids and Some Chemical Properties of the Vinylphenols, J. Am. Chem. Soc., 1958, 80, 3645. [all data]

Smith and Niederl, 1931
Smith, R.A.; Niederl, J.B., Reactions of Heterocycles with Phenols. Studies in the Reaction of Ethylene Oxide with Phenol, J. Am. Chem. Soc., 1931, 53, 806. [all data]

Sing, Smadja, et al., 1992
Sing, A.S.C.; Smadja, J.; Brevard, H.; Maignial, L.; Chaintreau, A.; Marion, J.-P., Volatile constituents of faham (Jumellea fragrans (Thou.) Schltr.), J. Agric. Food Chem., 1992, 40, 4, 642-646, https://doi.org/10.1021/jf00016a024 . [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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