Ethyl chloroacetate
From Wikipedia, the free encyclopedia
| Names | |
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| Preferred IUPAC name
Ethyl chloroacetate | |
Other names
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| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.995 Edit this at Wikidata |
| EC Number |
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PubChem CID |
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| UNII | |
| UN number | 1181 |
CompTox Dashboard (EPA) |
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| Properties | |
| ClCH2CO2CH2CH3 | |
| Molar mass | 122.55g·mol−1 |
| Density | 1.145 g/mL[1] |
| Melting point | −26°C (−15°F; 247K)[1] |
| Boiling point | 143°C (289°F; 416K)[1] |
| −72.3·10−6 cm3/mol | |
| Hazards | |
| GHS labelling:[2] | |
| GHS06: Toxic GHS09: Environmental hazard | |
| Danger | |
| H301, H311, H331, H400 | |
| P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P316, P321, P330, P361+P364, P391, P403+P233, P405, P501 | |
| Related compounds | |
Related esters |
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Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25°C [77°F], 100kPa).
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Chemical compound
Ethyl chloroacetate is an organic compound with the chemical formula Cl C H 2CO 2CH2CH3. It is used primarily in the chemical industry. It is used as a solvent for organic synthesis and as an intermediate in the production of pesticides (such as sodium fluoroacetate).[3]
Use
[edit ]- An example for the use of this agent was in the synthesis of cinepazet.
- Synthesis of Fenmetramide.
References
[edit ]- 1 2 3 Ethyl chloroacetate at Sigma-Aldrich
- ↑ "Ethyl chloroacetate". pubchem.ncbi.nlm.nih.gov.
- ↑ "Ethyl chloroacetate" (PDF). U.S. Environmental Protection Agency . April 2009.[dead link ]
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