Global InformationVinylene carbonate information
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| Names | |
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| Preferred IUPAC name
2H-1,3-Dioxol-2-one | |
| Other names
1,3-Dioxolene-2-one
Vinyl carbonate | |
| Identifiers | |
CAS Number
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3D model (JSmol)
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| ChemSpider |
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| ECHA InfoCard | 100.011.659 |
| EC Number |
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PubChem CID
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| UNII |
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CompTox Dashboard (EPA)
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InChI
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SMILES
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| Properties | |
Chemical formula
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C3H2O3 |
| Molar mass | 86.05 g·mol−1 |
| Appearance | colourless liquid[1] |
| Density | 1.35 |
| Melting point | 22 °C (72 °F; 295 K) |
| Boiling point | 178 °C (352 °F; 451 K)[2] |
| Hazards | |
| GHS labelling: | |
Pictograms
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Signal word
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Danger |
Hazard statements
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H302, H311, H315, H317, H318, H373, H411 |
Precautionary statements
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P260, P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P305+P351+P338, P310, P312, P314, P321, P322, P330, P332+P313, P333+P313, P361, P362, P363, P391, P405, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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Vinylene carbonate (VC) or 1,3-dioxol-2-one, is the simplest unsaturated cyclic carbonic acid ester. Vinylene carbonate can also be thought of as the cyclic carbonate of the hypothetical (Z)-ethene-1,2-diol. The activated double bond in this five-membered oxygen-containing heterocycle makes the molecule a reactive monomer for homopolymerization and copolymerization and a dienophile in Diels-Alder reactions. Below room temperature vinylene carbonate is a colorless stable solid.
- ^ Sigma-Aldrich Co., product no. {{{id}}}.
- ^ Haynes, W. M., ed. (2016). CRC Handbook of Chemistry and Physics (96th ed.). Boca Raton, Florida: CRC Press/Taylor & Francis. p. 3-228. ISBN 978-1482260960.