Butane, 1-(ethylsulfonyl)-

• Formula: C₆H₁₄O₂S
• Molecular weight: 150.239
• IUPAC Standard InChI: InChI=1S/C6H14O2S/c1-3-5-6-9(7,8)4-2/h3-6H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: PVSJGAIWOIMZFG-UHFFFAOYSA-N Copy
• CAS Registry Number: 31124-38-6
• 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: Sulfone, butyl ethyl; Butyl ethyl sulfone
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• Information on this page:
  • Phase change data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
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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: 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.

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]

Michalski, Wieczorkowski, et al., 1958
Michalski, J.; Wieczorkowski, J.; Modro, T., Reactions of Alkyl Alkanethioculfonates with Trialkyl Phosphites. A New Synthesis of O,O,S-Trialkyl Thiophosphates and Esters of Alkanesulfinic Acids, Roczniki Chem., 1958, 32, 1409-11. [all data]

Idson and Spoerri, 1954
Idson, B.; Spoerri, P.E., 1,4-Thiazans I. C-Alkyl Thiomorpholines, J. Am. Chem. Soc., 1954, 76, 2902-6. [all data]

Mcallan, Cullum, et al., 1951
Mcallan, D.T.; Cullum, T.V.; Dean, R.A.; Fidler, F.A., The Preparation and Properties of Sulfur Compounds Related to Petroleum I. The Dialkyl Sulfides and Disulfides, J. Am. Chem. Soc., 1951, 73, 3627-32. [all data]

Harmon, 1945
Harmon, J., , 1945. [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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