Thiirane, (methoxymethyl)-

• Formula: C₄H₈OS
• Molecular weight: 104.171
• IUPAC Standard InChI: InChI=1S/C4H8OS/c1-5-2-4-3-6-4/h4H,2-3H2,1H3 Copy

  
• IUPAC Standard InChIKey: SVUNGRWSYPGFNP-UHFFFAOYSA-N Copy
• CAS Registry Number: 19858-14-1
• 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: 2,3-Epithiopropyl methyl ether; Ether, 2,3-epithiopropyl methyl; (Methoxymethyl)thiirane; 2-(Methoxymethyl)thiirane; Thiirane, 2-(methoxymethyl)-; 2,3-Epithiopropyl methoxy ether
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Mass spectrum (electron ionization)
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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 as indicated in comments:
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C₄H₈OS⁺ (ion structure unspecified)

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]

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]

Notes

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