Chemistry:Methyl propiolate
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| Names | |
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| Preferred IUPAC name
Methyl prop-2-ynoate | |
| Other names
methyl propynoate
methyl acetylenecarboxylate | |
| Identifiers | |
3D model (JSmol)
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| 4-02-00-01688 | |
| ChemSpider | |
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PubChem CID
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| Properties | |
| C4H4O2 | |
| Molar mass | 84.074 g·mol−1 |
| Appearance | colorless liquid |
| Density | 0.945 g mL−1 |
| Boiling point | 103–105 °C (217–221 °F; 376–378 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Methyl propiolate is an organic compound with the formula HC2CO2CH3. It is the methyl ester of propiolic acid, the simplest acetylenic carboxylic acid. It is a colorless liquid that is miscible with organic solvents. The compound is a reagent and building block for the synthesis of other organic compounds, reactions that exploit the electrophilicity of the alkyne group.[1]
References
- ↑ Hirst, Gavin C. (2001). "Encyclopedia of Reagents for Organic Synthesis". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rm237. ISBN 0471936235.
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