Ethyl chloroacetate

Ethyl chloroacetate
Names
	Preferred IUPAC name Ethyl chloroacetate
	Other names Ethyl 2-chloroacetate; Ethyl monochloroacetate
Identifiers
CAS Number	105-39-5;
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL3186148;
ChemSpider	7465;
ECHA InfoCard	100.002.995
EC Number	203-294-0;
PubChem CID	7751;
UNII	6H07TEH4TF ;
UN number	1181
CompTox Dashboard (EPA)	DTXSID4026715 ;
	InChI InChI=1S/C4H7ClO2/c1-2-7-4(6)3-5/h2-3H2,1H3 Key: VEUUMBGHMNQHGO-UHFFFAOYSA-N; InChI=1/C4H7ClO2/c1-2-7-4(6)3-5/h2-3H2,1H3 Key: VEUUMBGHMNQHGO-UHFFFAOYAS;
	SMILES ClCC(=O)OCC;
Properties
Chemical formula	C4H7ClO2
Molar mass	122.55 g·mol−1
Density	1.145 g/mL
Melting point	−26 °C (−15 °F; 247 K)
Boiling point	143 °C (289 °F; 416 K)
Magnetic susceptibility (χ)	-72.3·10−6 cm3/mol
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H301, H311, H331, H400
Precautionary statements	P261, P262, P264, P270, P271, P273, P280, P301+P316, P302+P352, P304+P340, P316, P321, P330, P361+P364, P391, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Ethyl chloroacetate is a chemical compound 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]

An example for the use of this agent was in the synthesis of Cinepazet.

References

^ ^a ^b ^c Ethyl chloroacetate at Sigma-Aldrich
^ "Ethyl chloroacetate". pubchem.ncbi.nlm.nih.gov.
^ "Ethyl chloroacetate" (PDF). U.S. Environmental Protection Agency. April 2009.^{[permanent dead link‍]}

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[Aldrich-1] Ethyl chloroacetate at Sigma-Aldrich

[2] "Ethyl chloroacetate". pubchem.ncbi.nlm.nih.gov.

[3] "Ethyl chloroacetate" (PDF). U.S. Environmental Protection Agency. April 2009.^{[permanent dead link‍]}

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