(E)-1-Phenyl-1-butene
- Formula: C10H12
- Molecular weight: 132.2023
- IUPAC Standard InChIKey: MPMBRWOOISTHJV-XVNBXDOJSA-N
- CAS Registry Number: 1005-64-7
- 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:
- Other names: Benzene, 1-butenyl-, (E)-; trans-1-Phenyl-1-butene; 1-phenyl-(E)-1-butene
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Phase change data
Go To: Top, Gas phase ion energetics data, References, Notes
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
Quantity | Value | Units | Method | Reference | Comment |
---|---|---|---|---|---|
Tboil | 471.9 | K | N/A | Weast and Grasselli, 1989 | BS |
Tboil | 473.15 | K | N/A | Overberger and Tanner, 1955 | Uncertainty assigned by TRC = 2. K; TRC |
Tboil | 471.85 | K | N/A | Anonymous, 1952 | Uncertainty assigned by TRC = 0.5 K; TRC |
Tboil | 470.25 | K | N/A | Ward and Fulweiler, 1934 | Uncertainty assigned by TRC = 1. K; TRC |
Quantity | Value | Units | Method | Reference | Comment |
Tfus | 230.05 | K | N/A | Anonymous, 1952 | Uncertainty assigned by TRC = 0.3 K; TRC |
Gas phase ion energetics data
Go To: Top, Phase change data, References, Notes
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:
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
View reactions leading to C10H12+ (ion structure unspecified)
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
8.0 | PE | Kobayashi, Arai, et al., 1981 | LLK |
8.30 | PE | Kobayashi, Arai, et al., 1981 | Vertical value; LLK |
References
Go To: Top, Phase change data, Gas phase ion energetics data, Notes
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]
Overberger and Tanner, 1955
Overberger, C.G.; Tanner, D.,
Ionic Polymerization. A Convenient Synthesis of a.pha.- and β- Alkylstyrenes. THe Effect of an α-Alkyl Group on the Ultraviolet Absorption Spectra,
J. Am. Chem. Soc., 1955, 77, 369. [all data]
Anonymous, 1952
Anonymous, R.,
, Physical Properties of Chemical Substances, Dow Chemical Co., 1952. [all data]
Ward and Fulweiler, 1934
Ward, A.L.; Fulweiler, W.H.,
Ind. Eng. Chem., Anal. Ed., 1934, 6, 396. [all data]
Kobayashi, Arai, et al., 1981
Kobayashi, T.; Arai, T.; Sakuragi, H.; Tokumaru, K.; Utsunomiya, C.,
A new nethod for conformational analysis by photoelectron spectroscopy with application to alkyl-substituted styrenes,
Bull. Chem. Soc. Jpn., 1981, 54, 1658. [all data]
Notes
Go To: Top, Phase change data, Gas phase ion energetics data, References
- Symbols used in this document:
Tboil Boiling point Tfus Fusion (melting) point - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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