Ascaridole

• Formula: C₁₀H₁₆O₂
• Molecular weight: 168.2328
• IUPAC Standard InChI: InChI=1S/C10H16O2/c1-8(2)10-6-4-9(3,5-7-10)11-12-10/h4,6,8H,5,7H2,1-3H3 Copy

  
• IUPAC Standard InChIKey: MGYMHQJELJYRQS-UHFFFAOYSA-N Copy
• 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:
  • trans-Ascaridole
• Stereoisomers:
  • (Z)-Ascaridole
  • cis-isoascaridole
  • Isoascaridole
• 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
• Information on this page:
  • Phase change data
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
  • Gas Chromatography
• Options:
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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 by: Robert L. Brown and Stephen E. Stein

Reduced pressure boiling point

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 by: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

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.

Buckingham and Donaghy, 1982
Buckingham, J.; Donaghy, S.M., Dictionary of Organic Compounds: Fifth Edition, Chapman and Hall, New York, 1982, 1. [all data]

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]

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, 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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