1-Hexene, 5-methyl-

• Formula: C₇H₁₄
• Molecular weight: 98.1861
• IUPAC Standard InChI: InChI=1S/C7H14/c1-4-5-6-7(2)3/h4,7H,1,5-6H2,2-3H3 Copy

  
• IUPAC Standard InChIKey: JIUFYGIESXPUPL-UHFFFAOYSA-N Copy
• CAS Registry Number: 3524-73-0
• 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: 5-Methyl-1-hexene; 5-methylhex-1-ene
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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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 as indicated in comments:
BS - Robert L. Brown and Stephen E. Stein
TRC - 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.

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]

Chel'tsova, Chernyshev, et al., 1955
Chel'tsova, M.A.; Chernyshev, E.A.; Petrov, A.D., Behaviour of Alkenyl Halides with Unsaturated Bond in γ-, δ, ε-Postion in Condenstation Reactions with Alkyl Halides in the Presence of Magnesium, Izv. Akad. Nauk SSSR, 1955, 1955, 522-7. [all data]

Heller, 1952
Heller, H.E., The Racemization of d(+)-3-Methylhexane, J. Am. Chem. Soc., 1952, 74, 4858. [all data]

Rowlands, Greenlee, et al., 1952
Rowlands, D.C.; Greenlee, K.W.; Derfer, J.M.; Boord, C.E., The Use of Alkyl Vinyl Ethers in Olefin Synthesis, J. Org. Chem., 1952, 17, 807-11. [all data]

Anonymous, 1950
Anonymous, R., , Am. Pet. Inst. Res. Proj. 6, Natl. Bur. Stand., 1950. [all data]

Boord, Greenlee, et al., 1950
Boord, C.E.; Greenlee, K.W.; Derfer, J.M., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Wt., Am. Pet. Inst. Res. Proj. 45, Twelfth Annu. Rep., Ohio State Univ., 1950. [all data]

Anonymous, 1949
Anonymous, R., , Am. Pet. Inst. Res. Proj. 45, Ohio State Univ., 1949. [all data]

Anonymous, 1945
Anonymous, R., Private Commun., Am. Pet. Inst. Res. Proj. 45, 1945. [all data]

Beltz, 1939
Beltz, J.C., , Diss. Abstr. No. 28, 1939. [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]

Mulliken, Wakeman, et al., 1935
Mulliken, S.P.; Wakeman, R.L.; Gerry, H.T., The preparation of certain alkenes, alkadienes and alkynes, J. Am. Chem. Soc., 1935, 57, 1605-7. [all data]

Soday and Boord, 1933
Soday, F.J.; Boord, C.E., Synthesis in the Olefin Series IV. The Heptenes, J. Am. Chem. Soc., 1933, 55, 3293. [all data]

Dykstra, Lewis, et al., 1930
Dykstra, H.B.; Lewis, J.F.; Boord, C.E., A nuclear synthesis of unsaturated hydrocarbons: I alpha-olefins, J. Am. Chem. Soc., 1930, 52, 3396. [all data]

Swallen and Boord, 1930
Swallen, L.C.; Boord, C.E., J. Am. Chem. Soc., 1930, 52, 651-60. [all data]

Brooks and Humphrey, 1918
Brooks, B.T.; Humphrey, I., The Action of Concentrated Sulfuric Acid on Olefins, with Particular Reference to the Refining of Petroleum Distillates, J. Am. Chem. Soc., 1918, 40, 822. [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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