Stilbene

• Formula: C₁₄H₁₂
• Molecular weight: 180.2451
• IUPAC Standard InChI: InChI=1S/C14H12/c1-3-7-13(8-4-1)11-12-14-9-5-2-6-10-14/h1-12H Copy

  
• IUPAC Standard InChIKey: PJANXHGTPQOBST-UHFFFAOYSA-N Copy
• CAS Registry Number: 588-59-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • (E)-Stilbene
  • cis-Stilbene
• Other names: 1,2-Diphenylethylene; Benzene, 1,1'-(1,2-ethenediyl)bis-; Bibenzal; Bibenzylidene; Bibenzylidine; α,β-Diphenylethylene; Stilben; 1,2-Diphenylethene; 1,1'-(1,2-Ethenediyl)bis[benzene]; (2-Phenylethenyl)benzene
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Gas phase ion energetics data
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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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.

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

Hauptmann and Wladislaw, 1950
Hauptmann, H.; Wladislaw, B., The Action of Raney Nickel upon Sulfur Compounds II. Mercaptals, Mercaptols and Disulfides, J. Am. Chem. Soc., 1950, 72, 707. [all data]

Pearl and Dehn, 1938
Pearl, I.A.; Dehn, W.M., Reduction fo Benzil, J. Am. Chem. Soc., 1938, 60, 57. [all data]

Timmermans, 1935
Timmermans, J., Researches in Stoichiometry. I. The Heat of Fusion of Organic Compounds., Bull. Soc. Chim. Belg., 1935, 44, 17-40. [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]

Kern, Shriner, et al., 1925
Kern, J.W.; Shriner, R.L.; Adams, R., Platinum and Palladium Oxides as Catalysts in the Reduction of Organic Compounds IX. The Reduction of Olefins, J. Am. Chem. Soc., 1925, 47, 1147. [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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