Benzene, 1,1',1'',1'''-(1,2-ethenediylidene)tetrakis-

• Formula: C₂₆H₂₀
• Molecular weight: 332.4370
• IUPAC Standard InChI: InChI=1S/C26H20/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22)26(23-17-9-3-10-18-23)24-19-11-4-12-20-24/h1-20H Copy

  
• IUPAC Standard InChIKey: JLZUZNKTTIRERF-UHFFFAOYSA-N Copy
• CAS Registry Number: 632-51-9
• Chemical structure:
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• Other names: Ethylene, tetraphenyl-; Tetraphenylethene; Tetraphenylethylene; 1,1,2,2-Tetraphenylethylene; α,β-Diphenylstilbene; 1,1,2,2-Tetraphenylethene
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
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Normal melting point

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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

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.

Hauser, Brasen, et al., 1956
Hauser, C.R.; Brasen, W.R.; Skell, P.S.; Kantor, S.W.; Brodhag, A.E., Dimeric Oleifins versus AMins from α-Aryl Alkyl Halides with Alkali Dehydrohalogenation. Imines from Amines, J. Am. Chem. Soc., 1956, 78, 1653-8. [all data]

Sangster and Irvine, 1956
Sangster, R.C.; Irvine, J.W., Study of Organic Scintillators, J. Chem. Phys., 1956, 24, 670. [all data]

McGrath and Levine, 1955
McGrath, T.F.; Levine, R., The Reactions of Certain Fluorinated and Chlorinated Acetic Acids with Phenyllithium in Refluxing Ether, J. Am. Chem. Soc., 1955, 77, 3634. [all data]

Milas, Davis, et al., 1955
Milas, N.A.; Davis, P.; Nolan, J.T., Organic Peroxides XX. Peroxides from the Ozonization of Olefins in the Presence of Carbonium Ions, J. Am. Chem. Soc., 1955, 77, 2536. [all data]

Zartman and Adkins, 1932
Zartman, W.H.; Adkins, H., J. Am. Chem. Soc., 1932, 54, 1668. [all data]

Smith and Andrews, 1931
Smith, R.H.; Andrews, D.H., Thermal Energy Studies I. Phenyl Derivatives of Methane, Ethane and Some Related Compounds, J. Am. Chem. Soc., 1931, 53, 3644. [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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