2,4-Heptadiene

• Formula: C₇H₁₂
• Molecular weight: 96.1702
• IUPAC Standard InChI: InChI=1S/C7H12/c1-3-5-7-6-4-2/h3,5-7H,4H2,1-2H3 Copy

  
• IUPAC Standard InChIKey: XTJLXXCARCJVPJ-UHFFFAOYSA-N Copy
• CAS Registry Number: 628-72-8
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
  The 3d structure may be viewed using Java or Javascript.
• Stereoisomers:
  • 2,4-Heptadiene, (E,E)-
  • 2,4-Heptadiene, (Z,Z)
  • 2,4-Heptadiene, (Z,E)
  • 2,4-Heptadiene, (E,Z)
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• Information on this page:
  • Phase change data
  • Gas Chromatography
  • References
  • Notes
• Other data available:
  • Gas phase ion energetics data
  • UV/Visible 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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

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, temperature ramp

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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.

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]

Gorin and Vasil'eva, 1954
Gorin, Yu.A.; Vasil'eva, F.A., Zh. Obshch. Khim., 1954, 24, 1795. [all data]

Henne and Turk, 1942
Henne, A.L.; Turk, A., Conjugated diolefins by double bond displacement, J. Am. Chem. Soc., 1942, 64, 826-8. [all data]

Karasev and Khabarova, 1940
Karasev, K.I.; Khabarova, Zh. Obshch. Khim., 1940, 10, 1641. [all data]

Reif, 1908
Reif, J., The effect of magnesium organic compounds on orotonaldehyde (2-butene), and the optic behavior of the products, Ber. Dtsch. Chem. Ges., 1908, 41, 2739-46. [all data]

Chupalov and Zenkevich, 1996
Chupalov, A.A.; Zenkevich, I.G., Chromatographic Characterization of Structural Transformations of Organic Compounds in Diels-Alder Reaction. Aliphatic Dienes and Dienophyls, Zh. Org. Khim., 1996, 32, 6, 675-684. [all data]

Notes

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• Symbols used in this document:
  

  Tboil

  Boiling point

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