Oxirane, phenyl-
- Formula: C8H8O
- Molecular weight: 120.1485
- IUPAC Standard InChIKey: AWMVMTVKBNGEAK-UHFFFAOYSA-N
- CAS Registry Number: 96-09-3
- 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, (epoxyethyl)-; α,β-Epoxystyrene; (Epoxyethyl)benzene; (1,2-Epoxyethyl)benzene; Epoxystyrene; Phenethylene oxide; Phenylethylene oxide; Phenyloxirane; Styrene epoxide; Styrene oxide; Styrene 7,8-oxide; Styryl oxide; 1-Phenyl-1,2-epoxyethane; 1-Phenyloxirane; 2-Phenyloxirane; NCI-C54977; 1,2-Epoxy-1-phenylethane; Fenyloxiran; Ethane, 1,2-epoxy-1-phenyl-; NSC 637; Oxirane, 2-phenyl-; (.+/-.)-Styrene oxide; Benzene, epoxymethyl-
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Gas phase ion energetics data
Go To: Top, Gas Chromatography, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi
View reactions leading to C8H8O+ (ion structure unspecified)
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
9.23 | PE | Akiyama, Li, et al., 1979 | Vertical value |
9.04 | PE | Shudo, Kobayashi, et al., 1977 | Vertical value |
9.07 | PE | McAlduff and Houk, 1977 | Vertical value |
Gas Chromatography
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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: NIST Mass Spectrometry Data Center, William E. Wallace, director
Kovats' RI, polar column, isothermal
Column type | Active phase | Temperature (C) | I | Reference | Comment |
---|---|---|---|---|---|
Capillary | Carbowax 20M | 110. | 1630.8 | Boneva and Vassilev, 1996 | 50. m/0.32 mm/0.3 μm, N2 |
Capillary | Carbowax 20M | 120. | 1628.9 | Boneva and Vassilev, 1996 | 50. m/0.32 mm/0.3 μm, N2 |
Normal alkane RI, non-polar column, temperature ramp
Column type | Active phase | I | Reference | Comment |
---|---|---|---|---|
Capillary | HP-5 | 1119. | Kucuk, Gulec, et al., 2006 | 30. m/0.32 mm/0.25 μm, Helium, 60. C @ 2. min, 5. K/min, 260. C @ 13. min |
References
Go To: Top, Gas phase ion energetics data, Gas Chromatography, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Akiyama, Li, et al., 1979
Akiyama, I.; Li, K.C.; LeBreton, P.R.; Fu, P.P.; Harvey, R.G.,
Ultraviolet photoelectron studies of polycyclic aromatic hydrocarbons. The ground-state electronic structure of aryloxiranes and metabolites of benzo[a]pyrene,
J. Phys. Chem., 1979, 83, 2997. [all data]
Shudo, Kobayashi, et al., 1977
Shudo, K.; Kobayashi, T.; Utsunomiya, C.,
Photoelectron spectral studies on the interaction of three-membered rings with aryl groups,
Tetrahedron, 1977, 33, 1721. [all data]
McAlduff and Houk, 1977
McAlduff, E.J.; Houk, K.N.,
Photoelectron spectra of substituted oxiranes and thiiranes. Substituent effects on ionization potentials involving σ orbitals,
Can. J. Chem., 1977, 55, 318. [all data]
Boneva and Vassilev, 1996
Boneva, S.; Vassilev, K.,
Gas chromatographic separation of epoxystyrenes on carbowax 20 M capillary column,
Chromatographia, 1996, 43, 3/4, 208-210, https://doi.org/10.1007/BF02292953
. [all data]
Kucuk, Gulec, et al., 2006
Kucuk, M.; Gulec, C.; Yasar, A.; Ucuncu, O.; Yayh, N.; Coskuncelebi, K.; Terzioglu, S.; Yayh, N.,
Chemical composition and antimicrobial activities of the essential oils of Teucrium chamaedrys subsp. chamaedrys, T. orientale var. puberulens, and T. chamaedrys subsp. lydium,
Pharm. Biol., 2006, 44, 8, 592-599, https://doi.org/10.1080/13880200600896868
. [all data]
Notes
Go To: Top, Gas phase ion energetics data, Gas Chromatography, References
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