1-Pentene, 4,4-dimethyl-

• Formula: C₇H₁₄
• Molecular weight: 98.1861
• IUPAC Standard InChI: InChI=1S/C7H14/c1-5-6-7(2,3)4/h5H,1,6H2,2-4H3 Copy

  
• IUPAC Standard InChIKey: KLCNJIQZXOQYTE-UHFFFAOYSA-N Copy
• CAS Registry Number: 762-62-9
• 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-Dimethyl-4-pentene; 4,4-Dimethyl-1-pentene; (CH3)3CCH2CH=CH2; 4,4-dimethylpent-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
  • Gas phase ion energetics data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
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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]

Anonymous, 1962
Anonymous, R., , Am. Pet. Inst. Res. Proj. 58A, Annu. Rep., 1962. [all data]

Desty and Whyman, 1957
Desty, D.H.; Whyman, B.H.F., Anal. Chem., 1957, 29, 320. [all data]

Robertson, Heyes, et al., 1952
Robertson, P.W.; Heyes, J.K.; Swedlund, B.E., The Kinetics of Halogen Addition to Unsaturated Compounds XXII. Alkyl- and Halogenoalkylethylenes, J. Chem. Soc., 1952, 1952, 1014. [all data]

Anonymous, 1951
Anonymous, R., , Sunbury Rep. No. 4199, Anglo-Iranian Oil Co., 1951. [all data]

Glasgow, 1951
Glasgow, A.R., J. Res. Natl. Bur. Stand. (U. S.), 1951, 46, 43. [all data]

Braun, Spooner, et al., 1950
Braun, W.G.; Spooner, D.F.; Fenske, M.R., Raman spectra hydrocarbons and oxygenated compounds, Anal. Chem., 1950, 22, 1074. [all data]

Boord, Henne, et al., 1949
Boord, C.E.; Henne, A.L.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Grignard Reagent in hydrocarbon synthesis, Ind. Eng. Chem., 1949, 41, 609. [all data]

Boord, Greenlee, et al., 1948
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L.; Derfer, J.M., The Synthesis, Purificaiton and Prop. of Hydrocarbons of Low Mol. Wt., Am. Pet. Inst. Res. Proj. 45, Tenth Annu. Rep., Ohio State Univ., 1948. [all data]

Boord, Greenlee, et al., 1946
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L., The Synthesis, Purification and Prop. of Hydrocarbons of Low Mol. Weight, Am. Pet. Inst. Res. Proj. 45, Eighth Annu. Rep., Ohio State Univ., June 30, 1946. [all data]

Schmerling, 1946
Schmerling, L., Condensation of Saturated Halides with Unsaturated Compounds II. The Condensation of ALkyl Halides with Monohaloolefins, J. Am. Chem. Soc., 1946, 68, 1650-4. [all data]

Boord, Greenlee, et al., 1945
Boord, C.E.; Greenlee, K.W.; Perilstein, W.L., , Am. Pet. Inst. Res. Proj. 45, Seventh Annu. Rep., Ohio State Univ., June 30, 1945. [all data]

Schmerling, 1945
Schmerling, L., J. Am. Chem. Soc., 1945, 67, 1438. [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]

Whitmore and Homeyer, 1933
Whitmore, F.C.; Homeyer, A.H., Preparation and Reactions of 4,4-Dimethylpentene-1 (Neopentylethylene), J. Am. Chem. Soc., 1933, 55, 4555. [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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