Butane, 1,1'-sulfonylbis-

• Formula: C₈H₁₈O₂S
• Molecular weight: 178.292
• IUPAC Standard InChI: InChI=1S/C8H18O2S/c1-3-5-7-11(9,10)8-6-4-2/h3-8H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: AIDFJGKWTOULTC-UHFFFAOYSA-N Copy
• CAS Registry Number: 598-04-9
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Butyl sulfone; Dibutyl sulfone; Dibutyl sulphone; 1,1'-Sulphonylbisbutane; Di-n-butyl sulfone; n-Butyl sulfone; 1-(Butylsulfonyl)butane; NSC 2116
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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
  • IR Spectrum
  • Mass spectrum (electron ionization)
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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]

Jarvis, Hoey, et al., 1988
Jarvis, W.T.; Hoey, M.D.; Finocchio, A.L.; Dittmar, D.C., Organic reactions of Reduced Species of Sulfur Dioxide, J. Org. Chem., 1988, 53, 5750-6. [all data]

Noureldin, McConnell, et al., 1984
Noureldin, N.A.; McConnell, W.B.; Lee, D.G., Heterogeneous Permanganate Oxidation. 4. The Oxidation of Sulfides and Selenides, Can. J. Chem., 1984, 62, 2113-6. [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]

Noureldin and Lee, 1982
Noureldin, N.A.; Lee, D.G., Heterogeneous Permanganate Oxidation 2. Oxidation of Alcohols Using Solid Hydrated Copper Permanganate, J. Org. Chem., 1982, 47, 2790-2. [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]

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]

Mackle and O'Hare, 1961
Mackle, H.; O'Hare, P.A.G., Studies in the thermochemistry of sulphones. Part 5.-Heats of combustion, formation, fusion, vaporization and atomization of eleven aliphatic sulphones, Trans. Faraday Soc., 1961, 57, 1070-1074. [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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