3-Heptene, 4-methyl-

• Formula: C₈H₁₆
• Molecular weight: 112.2126
• IUPAC Standard InChI: InChI=1S/C8H16/c1-4-6-8(3)7-5-2/h6H,4-5,7H2,1-3H3 Copy

  
• IUPAC Standard InChIKey: KKVVJQGDNYIIMN-UHFFFAOYSA-N Copy
• CAS Registry Number: 4485-16-9
• Chemical structure:
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• Stereoisomers:
  • 4-Methyl-trans-3-heptene
  • 4-Methyl-cis-3-heptene
  • (E)-4-Methylhept-3-ene
  • 3-Heptene, 4-methyl-, cis
• Other names: 4-Methyl-3-heptene
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
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Normal boiling 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

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

Buck, Elsner, et al., 1949
Buck, F.R.; Elsner, B.B.; Henshall, T.; Moore, T.S.; Murray, A.R.; Morrell, S.H.; Muller, G.; Plant, M.M.T.; Smith, J.C.; Wallsgrove, E.R., Hydrocarbon synthesis., J. Inst. Pet., 1949, 35, 631. [all data]

Komarewsky and Kritchevsky, 1943
Komarewsky, V.I.; Kritchevsky, T.H., Synthesis of Olefin Hydrocarbons by Catalytic Condensation and Dehydration of Aliphatic Aldehydes, J. Am. Chem. Soc., 1943, 65, 547-8. [all data]

Goldwasser and Taylor, 1939
Goldwasser, S.; Taylor, H.S., Catalytic dehydration of c6-c8 aliphatic alcohols, J. Am. Chem. Soc., 1939, 61, 1751. [all data]

Bjelouss, 1912
Bjelouss, E., The effect of grignard compounds on methyl ethyl acrolein and the production of some diolefins, olefins and saturated secondary alcohols, Ber. Dtsch. Chem. Ges., 1912, 45, 625. [all data]

Sokolov, 1889
Sokolov, E., J. Prakt. Chem., 1889, 39, 444. [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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