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Oxiranol is an organic chemical that is an alcohol derivative of oxirane: it consists of a hydroxy group as substituent on ethylene oxide. It can have two enantiomeric forms. The compound has been proposed as an intermediate in the interstellar formation of glycolaldehyde[1] (a constitutional isomer of oxiranol) and the oxidation of acrolein in the environment.[2]
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| Names | |
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| Preferred IUPAC name
Oxiranol | |
Other names
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| Identifiers | |
3D model (JSmol)
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C2H4O2 | |
| Molar mass | 60.052 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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References
edit- ^ Wang, Tianfang; Bowie, John H. (2010). "Radical routes to interstellar glycolaldehyde. The possibility of stereoselectivity in gas-phase polymerization reactions involving CH2O and ·CH2OH". Org. Biomol. Chem. 8 (20): 4757–4766. doi:10.1039/C0OB00125B. PMID 20714667.
- ^ Asatryan, Rubik; da Silva, Gabriel; Bozzelli, Joseph W. (2010). "Quantum Chemical Study of the Acrolein (CH2CHCHO) + OH + O2 Reactions". J. Phys. Chem. A. 114 (32): 8302–8311. Bibcode:2010JPCA..114.8302A. doi:10.1021/jp104828a. PMID 20701337.
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