o-Nitroaniline

• Formula: C₆H₆N₂O₂
• Molecular weight: 138.1240
• IUPAC Standard InChI: InChI=1S/C6H6N2O2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H,7H2 Copy

  
• IUPAC Standard InChIKey: DPJCXCZTLWNFOH-UHFFFAOYSA-N Copy
• CAS Registry Number: 88-74-4
• 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: Benzenamine, 2-nitro-; Aniline, o-nitro-; o-Aminonitrobenzene; Azoene Fast Orange GR Base; Azoene Fast Orange GR Salt; Azofix Orange GR Salt; Azogene Fast Orange GR; Brentamine Fast Orange GR Base; Brentamine Fast Orange GR Salt; C.I. Azoic Diazo Component 6; C.I. 37025; Devol Orange B; Devol Orange Salt B; Diazo Fast Orange GR; Fast Orange Base JR; Fast Orange GR Base; Fast Orange GR Salt; Fast Orange O Base; Fast Orange O Salt; Fast Orange Salt JR; Hiltonil Fast Orange GR Base; Hiltosal Fast Orange GR Salt; Hindasol Orange GR Salt; Natasol Fast Orange GR Salt; Orange Base Ciba II; Orange Base Irga II; Orange GRS Salt; Orange Salt Ciba II; Orange Salt Irga II; ONA; 1-Amino-2-Nitrobenzene; 2-Aminonitrobenzene; 2-Nitroaniline; 2-Nitrobenzenamine; 2-Nitro-benzeneamine; o-Nitraniline; Azoic Diazo Component 6; Fast Orange Base GR; Fast Orange Salt GR; Orthonitroaniline; 1-Nitro-2-aminobenzene; o-Nitranilin; NSC 9796
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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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:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
RDSH - Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

View reactions leading to C₆H₆N₂O₂⁺ (ion structure unspecified)

Ionization energy determinations

References

Go To: Top, Gas phase ion energetics data, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Potapov, Kardash, et al., 1972
Potapov, V.K.; Kardash, I.E.; Sorokin, V.V.; Sokolov, S.A.; Evlasheva, T.I., Photoionization of heteroaromatic compounds, Khim. Vys. Energ., 1972, 6, 392. [all data]

Crable and Kearns, 1962
Crable, G.F.; Kearns, G.L., Effect of substituent groups on the ionization potentials of benzenes, J. Phys. Chem., 1962, 66, 436. [all data]

Khalil, Meeks, et al., 1973
Khalil, O.S.; Meeks, J.L.; McGlynn, S.P., Electronic spectroscopy of highly polar aromatics. VII. Photoelectron spectra of nitroanilines, J. Am. Chem. Soc., 1973, 95, 5876. [all data]

Notes

Go To: Top, Gas phase ion energetics data, References

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