Juglone

• Formula: C₁₀H₆O₃
• Molecular weight: 174.1528
• IUPAC Standard InChI: InChI=1S/C10H6O3/c11-7-4-5-9(13)10-6(7)2-1-3-8(10)12/h1-5,12H Copy

  
• IUPAC Standard InChIKey: KQPYUDDGWXQXHS-UHFFFAOYSA-N Copy
• CAS Registry Number: 481-39-0
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: 1,4-Naphthalenedione, 5-hydroxy-; 1,4-Naphthoquinone, 5-hydroxy-; Akhnot; C.I. Natural Brown 7; C.I. 75500; Iuglon; Juglane; Juglon; Nucin; Regianin; Walnut Extract; Yuglon; 5-Hydroxy-1,4-naphthoquinone; 5-Hydroxynaphthoquinone; 8-Hydroxy-1,4-naphthoquinone; Jugnlon; NCI 2323; 1,4-Naphthoquinone, 8-hydroxy-; 5-Hydroxy-1,4-naftochinon; 5-Hydroxy-1,4-naphthalenedione; 5-Hydroxy-p-naphthoquinone; 8-Hydroxy-1,4-naphthalenedione; 1,4-Dihydro-1,4-dioxo-5-hydroxynaphthalene; NSC 153189; NSC 622948
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • 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 as indicated in comments:
LL - Sharon G. Lias and Joel F. Liebman
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

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.

Millefiori, Gulino, et al., 1990
Millefiori, S.; Gulino, A.; Casarin, M., UV Photoelectron spectra, reduction potentials and MO calculations of intramolecularly hydrogen-bonded naphtoquinones, J. Chim. Phys., 1990, 87, 317. [all data]

Potapov and Sorokin, 1971
Potapov, V.K.; Sorokin, V.V., Photoionization and ion-molecule reactions in quinones and alcohols, High Energy Chem., 1971, 5, 435, In original 487. [all data]

Notes

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