Indolizine

• Formula: C₈H₇N
• Molecular weight: 117.1479
• IUPAC Standard InChI: InChI=1S/C8H7N/c1-2-6-9-7-3-5-8(9)4-1/h1-7H Copy

  
• IUPAC Standard InChIKey: HOBCFUWDNJPFHB-UHFFFAOYSA-N Copy
• CAS Registry Number: 274-40-8
• 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: Pyrrolo[1,2-a]pyridine; Indolizin; Pyrrocolin; Pyrrocoline
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• Information on this page:
  • Phase change data
  • Gas phase ion energetics data
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • References
  • Notes
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Phase change 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: Robert L. Brown and Stephen E. Stein

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 evaluated as indicated in comments:
L - Sharon G. Lias

Data compiled as indicated in comments:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C₈H₇N⁺ (ion structure unspecified)

Ionization energy determinations

Mass spectrum (electron ionization)

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

UV/Visible spectrum

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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: Victor Talrose, Alexander N. Yermakov, Alexy A. Usov, Antonina A. Goncharova, Axlexander N. Leskin, Natalia A. Messineva, Natalia V. Trusova, Margarita V. Efimkina

Spectrum

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Additional Data

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.

Weast and Grasselli, 1989
CRC Handbook of Data on Organic Compounds, 2nd Editon, Weast,R.C and Grasselli, J.G., ed(s)., CRC Press, Inc., Boca Raton, FL, 1989, 1. [all data]

Corval, 1979
Corval, M., Elimination sous impact electronique de HCN et H a partir de l'Indole. Comparaison avec l'Indolizine, Org. Mass Spectrom., 1979, 14, 213. [all data]

Palmer, Leaver, et al., 1977
Palmer, M.H.; Leaver, D.; Nisbet, J.D.; Millar, R.W.; Egdell, R., The electronic structure of some J. Heterocycl. Chem. with bridgehead nitrogen: photoelectron spectra and ab initio molecular orbital calculations, J. Mol. Struct., 1977, 42, 85. [all data]

Kochetkova, 1963
Kochetkova, E.A., Zhur. Obshchei Khim. (in Rus.), 1963, 33, 1201. [all data]

Notes

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• Symbols used in this document:
  

  IE (evaluated)	Recommended ionization energy
  Tboil	Boiling point

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