Diphenyl sulfone

• Formula: C₁₂H₁₀O₂S
• Molecular weight: 218.272
• IUPAC Standard InChI: InChI=1S/C12H10O2S/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H Copy

  
• IUPAC Standard InChIKey: KZTYYGOKRVBIMI-UHFFFAOYSA-N Copy
• CAS Registry Number: 127-63-9
• 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: Benzene, 1,1'-sulfonylbis-; Phenyl sulfone; DPS; Sulfobenzide; Sulfone, diphenyl; Difenylsulfon; Diphenyl sulphone; Phenyl sulphone; (Phenylsulfonyl)benzene; NSC 627706; NSC 6780
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• Information on this page:
  • Normal melting point
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Gas phase ion energetics data
  • Ion clustering data
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Normal melting point

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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: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

References

Go To: Top, Normal melting point, Notes

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

Kaldor and Hammond, 1991
Kaldor, S.W.; Hammond, M., A Mild Osmium Tetraoxide-Catalyzed Method for the Oxidation of Sulfides to Sulfones, Tetrahedron Lett., 1991, 32, 5043-6. [all data]

Olah and Gupta, 1983
Olah, G.A.; Gupta, B.G.B., Onium Ions 27. Oxidation of Sulfoxides to Sulfones with Nitronium Salts, J. Org. Chem., 1983, 48, 3585-7. [all data]

Dyer, Harris, et al., 1982
Dyer, J.C.; Harris, D.L.; Evans, S.A., Oxygen-17 Nulcear Magnetic RFesonacne SPtroscopy of Sulfoxides and Sulfones. Alkyl Substituent Induced Chemical Shifts, J. Org. Chem., 1982, 47, 3660-4. [all data]

Venier, Squires, et al., 1982
Venier, C.G.; Squires, T.G.; Chen, Y. -Y; Hussmann, G.P.; Shei, J. C>; Smith, G.F., Peroxyfluoroacetic Acid. A Convenient Reagent for the Preparation of Sulfoxides and Sulfones, J. Org. Chem., 1982, 47, 3773-4. [all data]

Boehme and Sitorus, 1972
Boehme, V.H.; Sitorus, U., Oxidation of Thioethers to Sulfones with Hydrogen Peroxide in Alkaline Solution, Chem.-Ztg., 1972, 96, 37-8. [all data]

Graybill, 1967
Graybill, B.M., The Syntheses of Aryl Sulfones, J. Org. Chem., 1967, 32, 2931-3. [all data]

Hall and Robinson, 1964
Hall, S.K.; Robinson, E.A., The Sulphuric Acid Solvent System. Part VI. The Basicities of Compounds Containing Sulphur-Oxyten Bonds, Can. J. Chem., 1964, 42, 1113-22. [all data]

Hauptmann and Wladislaw, 1950
Hauptmann, H.; Wladislaw, B., The Action of Raney Nickel upon Sulfur Compounds II. Mercaptals, Mercaptols and Disulfides, J. Am. Chem. Soc., 1950, 72, 707. [all data]

Hauptmann and Wladislaw, 1950, 2
Hauptmann, H.; Wladislaw, B., The Action of Raney Nickel on SUlfur Compounds III. Aromatic Thioesters, J. Am. Chem. Soc., 1950, 72, 710. [all data]

Smith and Andrews, 1931
Smith, R.H.; Andrews, D.H., Thermal Energy Studies II. Phenyl Derivatives of Metals, J. Am. Chem. Soc., 1931, 53, 3661-7. [all data]

Notes

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• Symbols used in this document:
  

  Tfus	Fusion (melting) point

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