1H-Pyrrole, 1-phenyl-

• Formula: C₁₀H₉N
• Molecular weight: 143.1852
• IUPAC Standard InChI: InChI=1S/C10H9N/c1-2-6-10(7-3-1)11-8-4-5-9-11/h1-9H Copy

  
• IUPAC Standard InChIKey: GEZGAZKEOUKLBR-UHFFFAOYSA-N Copy
• CAS Registry Number: 635-90-5
• 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: Pyrrole, 1-phenyl-; N-Phenylpyrrole; 1-Phenylpyrrole
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• Information on this page:
  • Condensed phase thermochemistry data
  • Phase change data
  • References
  • Notes
• Other data available:
  • IR Spectrum
  • Mass spectrum (electron ionization)
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Condensed phase thermochemistry 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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - 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.

Stern and Klebs, 1933
Stern, A.; Klebs, G., Calorimetrische Bestimmungen bei einfachen und mehrkernigen Pyrrolderivaten, Ann., 1933, 504, 287-297. [all data]

Cox and Pilcher, 1970
Cox, J.D.; Pilcher, G., Thermochemistry of Organic and Organometallic Compounds, Academic Press, New York, 1970, 1-636. [all data]

Aldrich Chemical Company Inc., 1990
Aldrich Chemical Company Inc., Catalog Handbook of Fine Chemicals, Aldrich Chemical Company, Inc., Milwaukee WI, 1990, 1. [all data]

Cumper and Wood, 1971
Cumper, C.W.N.; Wood, J.W.M., Dielectric relaxation and dipole moments of substituted pyrroles., J. Chem. Soc. B, 1971, 1811. [all data]

Kofod, Sutton, et al., 1952
Kofod, H.; Sutton, L.E.; Jackson, J., The molecular structure of pyrrole and some of its simple derivatives, from electric dipole moment measurements, J. Chem. Soc., 1952, 1952, 1467. [all data]

Adkins and Coonradt, 1941
Adkins, H.; Coonradt, H.L., The Selective Hydrogenation of Derivatives of Pyrrole, Indole, Carbazole and Acridine, J. Am. Chem. Soc., 1941, 63, 1563-70. [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔcH°solid	Enthalpy of combustion of solid at standard conditions

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