trans-1,2-Diphenylethylene oxide

• Formula: C₁₄H₁₂O
• Molecular weight: 196.2445
• IUPAC Standard InChI: InChI=1S/C14H12O/c1-3-7-11(8-4-1)13-14(15-13)12-9-5-2-6-10-12/h1-10,13-14H/t13-,14-/m0/s1 Copy

  
• IUPAC Standard InChIKey: ARCJQKUWGAZPFX-KBPBESRZSA-N Copy
• CAS Registry Number: 1439-07-2
• Chemical structure:
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• Stereoisomers:
  • Bibenzyl, α,α'-epoxy-, cis-
  • Oxirane, 2,3-diphenyl-
• Other names: trans-Stilbene oxide; Oxirane, 2,3-diphenyl-, trans-; trans-Stilbene epoxide; trans-1,2-Diphenyloxirane; Bibenzyl, α,α'-epoxy-, trans-; Oxirane,trans-2,3-diphenyl-; 2,3-Diphenyloxirane, (E)-; NSC 100317; NSC 40295; Oxirane, 2,3-diphenyl-, (2R,3R)-rel-; trans-2,3-Diphenyloxirane; trans-α,α-epoxydibenzyl
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • IR Spectrum
  • Mass spectrum (electron ionization)
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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

View reactions leading to C₁₄H₁₂O⁺ (ion structure unspecified)

Ionization energy determinations

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.

Arnold and Wong, 1979
Arnold, D.R.; Wong, P.C., The oxidation potentials of cis- and trans-1,2-diphenylcyclo- propane and cis- and trans-2,3-diphenyloxirane, Can. J. Chem., 1979, 57, 2098. [all data]

Notes

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