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Ethyl chloroacetate information


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 Edit this at Wikidata
EC Number
  • 203-294-0
PubChem CID
  • 7751
UNII
  • 6H07TEH4TF checkY
UN number 1181
CompTox Dashboard (EPA)
  • DTXSID4026715 Edit this at Wikidata
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
ClCH2CO2CH2CH3
Molar mass 122.55 g·mol−1
Density 1.145 g/mL[1]
Melting point −26 °C (−15 °F; 247 K)[1]
Boiling point 143 °C (289 °F; 416 K)[1]
Magnetic susceptibility (χ)
−72.3·10−6 cm3/mol
Hazards
GHS labelling:[2]
Pictograms
GHS06: ToxicGHS09: Environmental hazard
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
Related compounds
Related esters
  • Ethyl bromoacetate
  • Ethyl 3-bromopropionate
  • Ethyl iodoacetate
  • Ethyl bromodifluoroacetate
  • Ethyl acetoacetate
Related compounds
  • Chloroacetic acid
  • Chloropicrin
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 an organic compound with the chemical formula ClCH2CO2CH2CH3. 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]

  1. ^ a b c 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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Ethyl chloroacetate

Last Update:

Ethyl chloroacetate is an organic compound with the chemical formula ClCH2CO2CH2CH3. It is used primarily in the chemical industry. It is used as a solvent...

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Sodium chloroacetate

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Sodium chloroacetate is the organic compound with the formula CH2ClCO2Na. A white, water-soluble solid, it is the sodium salt of chloroacetic acid. Many...

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Ethyl cyanoacetate

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and chemical reactivity. Ethyl cyanoacetate may be prepared in various ways: Kolbe nitrile synthesis using ethyl chloroacetate and sodium cyanide. Fischer...

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Diethyl malonate

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C2H5OH + 2 HCl → C2H5O2CCH2CO2C2H5 + NH4Cl + NaCl Alternatively, sodium chloroacetate undergoes carboxyesterification by treatment with carbon monoxide and...

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Bromobenzene

Last Update:

Refractive Index, and Speed of Sound in the Binary Mixtures of Ethyl Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol...

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Phendimetrazine

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phendimetrazine (4). The reaction between Ephedrine [299-42-3] (1) and ethyl chloroacetate [105-39-5] (2) in the presence of sodium hydride gives 4...

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Ethyl iodoacetate

Last Update:

Ethyl iodoacetate is an organic compound with the chemical formula ICH2CO2CH2CH3. It is a derivative of ethyl acetate. Under normal conditions, the compound...

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Ethyl bromoacetate

Last Update:

Ethyl bromoacetate is the chemical compound with the formula BrCH2CO2CH2CH3. It is the ethyl ester of bromoacetic acid and is prepared in two steps from...

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List of viscosities

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Refractive Index, and Speed of Sound in the Binary Mixtures of Ethyl Chloroacetate + Cyclohexanone, + Chlorobenzene, + Bromobenzene, or + Benzyl Alcohol...

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Brodifacoum

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obtain this starting Compound 1, a simple Wittig condensation of ethyl chloroacetate with 4’-bromobiphenylcarboxaldehyde is accomplished. Compound 1 is...

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Methyl chloroformate

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contact with water. It will cause skin damage if in contact with skin. Ethyl chloroacetate Chloroacetic acid Methyl chloroformate at Sigma-Aldrich Siegfried...

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Reformatsky reaction

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1002/cber.188702001268. Reformatsky, S. (1890). "Action of zinc and ethyl chloroacetate on ketones and aldehydes". J. Russ. Phys. Chem. Soc. 22: 44. Shriner...

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Nitro compound

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Nitromethane can be produced in the laboratory by treating sodium chloroacetate with sodium nitrite. Oxidation of oximes or primary amines. Reduction...

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List of compounds with carbon number 4

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chloride 141-75-3 C4H7ClO2 ethoxyacetyl chloride 500025-15-0 C4H7ClO2 ethyl chloroacetate 105-39-5 C4H7CsO2 caesium butyrate 38869-25-9 C4H7FO2 isopropyl fluoromethanoate...

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Cyanoacetamide

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by Fischer esterification and ester aminolysis. Chloroacetamide Ethyl chloroacetate Ibrahim, F.; Sharaf El-Din, M. K.; Eid, M.; Wahba, M. E. K. (2011)...

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Fenmetramide

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[154-41-6] was treated with NaH in mineral oil and later reacted with the ethyl chloroacetate [105-39-5]. Cis-product Ex 2: dl-norpseudoephedrine was used => trans-product...

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List of UN numbers 1101 to 1200

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2-Ethylbutyraldehyde UN 1179 3 Ethyl butyl ether UN 1180 3 Ethyl butyrate UN 1181 6.1 Ethyl chloroacetate UN 1182 6.1 Ethyl chloroformate UN 1183 4.3 Ethyldichlorosilane...

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Chloroacetic acid

Last Update:

046.0028; Collected Volumes, vol. 5, p. 251.. Inglis, J. K. H. (1928). "Ethyl Cyanoacetate". Organic Syntheses. 8: 74. doi:10.15227/orgsyn.008.0074. 40...

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Cyanoacetic acid

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components of adhesives. Cyanoacetic acid is prepared by treatment of chloroacetate salts with sodium cyanide followed by acidification. Electrosynthesis...

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List of UN numbers 2601 to 2700

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longer in use) Selenium (UN No. no longer in use) UN 2659 6.1 Sodium chloroacetate UN 2660 6.1 Nitrotoluidines (mono) UN 2661 6.1 Hexachloroacetone UN...

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List of compounds with carbon number 11

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undecanedioic acid 1852-04-6 C11H20O10 Sambubiose 26388-68-1 C11H21ClO2 nonyl chloroacetate 5451-96-7 C11H21N undecanenitrile 2244-07-7 C11H21NOS cycloate 1134-23-2...

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List of compounds with carbon number 14

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3674-07-5 C14H27ClO myristoyl chloride 112-64-1 C14H27ClO2 dodecyl chloroacetate 6316-04-7 C14H27N ethyldicyclohexylamine 7175-49-7 C14H27N tetradecanenitrile...

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Polyglycolide

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Polycondensation is carried out by heating an halogenoacetate, like sodium chloroacetate, at a temperature between 160 and 180 °C, continuously passing nitrogen...

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List of UN numbers 2901 to 3000

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N-Methylbutylamine UN 2946 6.1 2-Amino-5-diethylaminopentane UN 2947 3 Isopropyl chloroacetate UN 2948 6.1 3-Trifluoromethylaniline UN 2949 8 Sodium hydrosulfide,...

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List of compounds with carbon number 8

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bromoacetate 13048-32-3 C8H15ClO octanoyl chloride 111-64-8 C8H15ClO2 hexyl chloroacetate 5927-57-1 C8H15CoNO3P triethylphosphine cobalt dicarbonyl nitrosyl 21485-16-5...

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List of UN numbers 2201 to 2300

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4-Methoxy-4-methylpentan-2-one UN 2294 6.1 N-Methylaniline UN 2295 6.1 Methyl chloroacetate UN 2296 3 Methylcyclohexane UN 2297 3 Methylcyclohexanone UN 2298 3...

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List of compounds with carbon number 6

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C6H11ClO2 chloroacetic acid butyl ester 590-02-3 C6H11ClO2 sec butyl chloroacetate 17696-64-9 C6H11N hexanenitrile 628-73-9 C6H11N neopentyl cyanide 3302-16-7...

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List of compounds with carbon number 10

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phosphamidon 13171-21-6 C10H19ClO decanoyl chloride 112-13-0 C10H19ClO2 octyl chloroacetate 5451-98-9 C10H19N decanenitrile 1975-78-6 C10H19NO lupinine 486-70-4...

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