1H-Inden-1-one, 2,3-dihydro-

• Formula: C₉H₈O
• Molecular weight: 132.1592
• IUPAC Standard InChI: InChI=1S/C9H8O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4H,5-6H2 Copy

  
• IUPAC Standard InChIKey: QNXSIUBBGPHDDE-UHFFFAOYSA-N Copy
• CAS Registry Number: 83-33-0
• 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-Indanone; α-Hydrindone; α-Indanone; Indan-1-one; Indanone; 1-Indone; Indanone-(1); 2,3-Dihydro-1H-inden-1-one; 2,3-Dihydro-1-indenone; 2,3-Dihydro-1-indanone
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Gas phase ion energetics data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director
AC - William E. Acree, Jr., James S. Chickos

Reduced pressure boiling point

Enthalpy of vaporization

Enthalpy of fusion

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.

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

Huckel and Wenzke, 1944
Huckel, W.; Wenzke, U., The Association of Aromatic Alcohols, Z. Phys. Chem. (Leipzig), 1944, 193, 132-61. [all data]

Kadesch, 1944
Kadesch, R.G., Some New Aspects of the Ortho Effect. Cyclic Ketones Related to Acetophenone, J. Am. Chem. Soc., 1944, 66, 1207-13. [all data]

Von Auwers, 1918
Von Auwers, K., Justus Liebigs Ann. Chem., 1918, 415, 98. [all data]

Perkin, 1896
Perkin, W.H., LXIX. On Magnetic Rotatory Power, especially of Aromatic Compounds, J. Chem. Soc., 1896, 69, 1025-1257. [all data]

Matos, Miranda, et al., 2007
Matos, M. Agostinha R.; Miranda, Margarida S.; Pereira, Susana M.M.; Morais, Victor M.F.; Liebman, Joel F., The Experimental and Calculational Thermochemistry of 1,2,4,5-Benzenetetracarboxylic Dianhydride: Is This 10 π Multiring Species Aromatic?, J. Phys. Chem. A, 2007, 111, 30, 7181-7188, https://doi.org/10.1021/jp071625n . [all data]

Verevkin, 1998
Verevkin, S.P., Thermochemistry of aromatic ketones. Experimental enthalpies of formation and structural effects, Thermochim. Acta, 1998, 310, 229-235. [all data]

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]

Gudiño, Torres, et al., 1998
Gudiño, Ramón; Torres, Luis Alfonso; Santillán, Rosa Luisa; Farfán, Norberto, The standard molar enthalpies of combustion and vaporization of three oxazolidines, The Journal of Chemical Thermodynamics, 1998, 30, 6, 671-679, https://doi.org/10.1006/jcht.1997.0317 . [all data]

Notes

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• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point
  ΔfusH	Enthalpy of fusion
  ΔsubH°	Enthalpy of sublimation at standard conditions
  ΔvapH	Enthalpy of vaporization

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