1-Phenyl-1-butene

• Formula: C₁₀H₁₂
• Molecular weight: 132.2023
• IUPAC Standard InChI: InChI=1S/C10H12/c1-2-3-7-10-8-5-4-6-9-10/h3-9H,2H2,1H3 Copy

  
• IUPAC Standard InChIKey: MPMBRWOOISTHJV-UHFFFAOYSA-N Copy
• CAS Registry Number: 824-90-8
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Stereoisomers:
  • (E)-1-Phenyl-1-butene
  • Benzene, 1-butenyl-, (Z)-
• Other names: Benzene, 1-butenyl; β-Ethylstyrene; 1-Butenyl-benzene
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• Information on this page:
  • Normal boiling point
  • References
  • Notes
• Other data available:
  • Condensed phase thermochemistry data
  • Phase change data
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
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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.

Levi and Nicholls, 1958
Levi, L.; Nicholls, R.V.V., Formation of Styrene by Pyrolysis of Aromatic Heterocyclic Aldehyde- Aliphatic Acid Anhydride Mixtures on Morden Bentonite, Ind. Eng. Chem., 1958, 50, 1005. [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., 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]

Hurd and Bollman, 1933
Hurd, C.D.; Bollman, H.T., The Pyrolysis of Alpha Unsaturated Hydrocarbons, J. Am. Chem. Soc., 1933, 55, 699-702. [all data]

Boeseken and Blumberger, 1925
Boeseken, J.; Blumberger, J.S.P., Observation on the Speed of Oxidation of Several Aromatic Derivatives of Ethylene by the Prileshajew Reaction, Recl. Trav. Chim. Pays-Bas, 1925, 44, 90. [all data]

Klages, 1904
Klages, A., Ber. Dtsch. Chem. Ges., 1904, 37, 2301. [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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