Oxirane, [(2-propenyloxy)methyl]-

• Formula: C₆H₁₀O₂
• Molecular weight: 114.1424
• IUPAC Standard InChI: InChI=1S/C6H10O2/c1-2-3-7-4-6-5-8-6/h2,6H,1,3-5H2 Copy

  
• IUPAC Standard InChIKey: LSWYGACWGAICNM-UHFFFAOYSA-N Copy
• CAS Registry Number: 106-92-3
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Other names: Propane, 1-(allyloxy)-2,3-epoxy-; Allyl glycidyl ether; Allyl 2,3-epoxypropyl ether; Glycidyl allyl ether; 1-Allyloxy-2,3-epoxypropane; 1,2-Epoxy-3-allyloxypropane; Allylglycide ether; Allil-glicidil-etere; Allylglycidaether; AGE; Ether, allyl 2,3-epoxypropyl; M 560; Oxyde d'allyle et de glycidyle; 1-Allilossi-2,3 epossipropano; 1-Allyloxy-2,3-epoxy-propaan; 1-Allyloxy-2,3-epoxypropan; NCI-C56666; UN 2219; [(2-Propenyloxy)methyl]oxirane; Ageflex AGE; Sipomer AGE; NSC 18596; Oxirane, 2-[(2-propen-1-yloxy)methyl]-
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • Gas Chromatography
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Gas phase ion energetics data

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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: Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard

Ionization energy determinations

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.

Rodin, Chistyakov, et al., 1985
Rodin, A.A.; Chistyakov, A.B.; Sarkisov, Y.S.; Sergeev, Y.L.; V'yunov, K.A.; Golovin, A.V., Electronic structure and geometric structure of three-member J. Heterocycl. Chem.. I. hotoelectron spectra of gylcidyl and thioglycidyl ethers, Russ. J. Phys. Chem., 1985, 59, 444, In original 764. [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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