Ascaridole
- Formula: C10H16O2
- Molecular weight: 168.2328
- IUPAC Standard InChIKey: MGYMHQJELJYRQS-UHFFFAOYSA-N
- CAS Registry Number: 512-85-6
- 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. - Species with the same structure:
- Stereoisomers:
- Other names: 2,3-Dioxabicyclo[2.2.2]oct-5-ene, 1-methyl-4-(1-methylethyl)-; p-Menth-2-ene, 1,4-epidioxy-; Ascaridol; Ascaricum; Ascarisin; Askaridol; 1,4-Peroxido-p-menthene-2; 1,4-Peroxy-p-menth-2-ene; 1,4-Epidioxy-p-menth-2-ene; 2,3-Dioxabicyclo(2.2.2)oct-5-ene, 1-isopropyl-4-methyl-; 1-Methyl-4-(1-methylethyl)-2,3-dioxabicyclo(2.2.2)oct-5-ene; Ascaridiol; NSC 406266; 1-Isopropyl-4-methyl-2,3-dioxabicyclo[2.2.2]oct-5-ene; Chenopodium oil; (Z)-Ascaridole; 1,4-epidioxy-2-p-menthene
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Gas phase ion energetics data
Go To: Top, 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
Ionization energy determinations
IE (eV) | Method | Reference | Comment |
---|---|---|---|
8.07 | PE | Brown, 1975 | |
8.42 | PE | Brown, 1976 | Vertical value |
References
Go To: Top, 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.
Brown, 1975
Brown, R.S.,
A photoelectron investigation of the peroxide bond,
Can. J. Chem., 1975, 53, 3439. [all data]
Brown, 1976
Brown, R.S.,
The influence of remote substituents upon ionization potential. Part I. The effect of two allylic oxygens upon the ionization of the π-bond,
Can. J. Chem., 1976, 54, 805. [all data]
Notes
Go To: Top, Gas phase ion energetics data, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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