Tetrahydrofuran, 2,2-dimethyl-

• Formula: C₆H₁₂O
• Molecular weight: 100.1589
• IUPAC Standard InChI: InChI=1S/C6H12O/c1-6(2)4-3-5-7-6/h3-5H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: ZPDIRKNRUWXYLJ-UHFFFAOYSA-N Copy
• CAS Registry Number: 1003-17-4
• 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: 2,2-Dimethyltetrahydrofuran
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• Information on this page:
  • Phase change data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Gas phase ion energetics data
  • IR Spectrum
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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

Mass spectrum (electron ionization)

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Spectrum

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Additional Data

Gas Chromatography

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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: NIST Mass Spectrometry Data Center, William E. Wallace, director

Normal alkane RI, non-polar column, custom temperature program

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References

Go To: Top, Phase change data, Mass spectrum (electron ionization), Gas Chromatography, Notes

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

Ansell and Thomas, 1958
Ansell, M.F.; Thomas, D.A., J. Chem. Soc., 1958, 1958, 1163. [all data]

Favorskaya and Shcherbinskaya, 1953
Favorskaya, T.A.; Shcherbinskaya, N.V., Zh. Obshch. Khim., 1953, 23, 1485. [all data]

Slabey and Wise, 1951
Slabey, V.A.; Wise, P.H., , Natl. Advis. Comm. Aeronaut., Tech. Notes, No. 2258, Lewis Fligt Propulsion Lab., Cleveland, OH, 1951. [all data]

Paul and Tchelitcheff, 1950
Paul, R.; Tchelitcheff, S., The Methylenyl-2-tetrahydrofuran. Application to the Preparation of beta-Ethylenic Alcohols. Synthesis of Sylvanne, Bull. Soc. Chim. Fr., 1950, 1950, 520. [all data]

Van Keersbilck, 1929
Van Keersbilck, N., Cyclopropane derivatives, Bull. Soc. Chim. Belg., 1929, 38, 205-11. [all data]

Farkas, Héberger, et al., 2004
Farkas, O.; Héberger, K.; Zenkevich, I.G., Quantitative structure-retention relationships. XIV. Prediction of gas chromatographic retention indices for saturated O-, N-, and S-heterocyclic compounds, Chemom. Intell. Lab. Syst., 2004, 72, 2, 173-184, https://doi.org/10.1016/j.chemolab.2004.01.012 . [all data]

Notes

Go To: Top, Phase change data, Mass spectrum (electron ionization), Gas Chromatography, References

• Symbols used in this document:
  

  Tboil	Boiling point
  Tfus	Fusion (melting) point

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