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Ethyl oxalyl chloride

Ethyl oxalyl chloride structure

Ethyl oxalyl chloride 

structure
  • CAS No:

    4755-77-5

  • Formula:

    C4H5ClO3

  • Chemical Name:

    Ethyl oxalyl chloride

  • Synonyms:

    Acetic acid,2-chloro-2-oxo-,ethyl ester;Acetic acid,chlorooxo-,ethyl ester;Glyoxylic acid,chloro-,ethyl ester;Ethoxalyl chloride;Ethyl 2-chloro-2-oxoacetate;Oxalic acid monoethyl ester chloride;Ethyl chloroglyoxylate;Ethyl oxalyl chloride;Ethyl chlorooxoacetate;Monoethyl oxaloyl chloride;Ethyl (chloroformyl)formate;Monoethyl oxalate monochloride;Oxalic acid monoethyl ester monochloride;Monoethyl oxalate chloride;Ethyl oxaloyl chloride;Oxalic acid ethyl ester chloride;Ethyl (chlorocarbonyl)carboxylate;Ethyl 2-chloro-2-oxoethanoate;Oxalic acid chloride ethyl ester;Chloroglyoxylic acid ethyl ester;NSC 80644;Chlorooxoacetic acid ethyl ester;1-(Chlorocarbonyl)formic acid ethyl ester;Oxalyl chloride ethyl ester;Ethoxyoxalyl chloride;Ethyl chlorooxalate;Ethyl oxalyl monochloride;Ethyl clorooxoacetate;Ethyl oxalochloridate

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

clear liquid

Ethyl oxalyl chloride Basic Attributes

136.53

136.53

506725

225-285-0

80644

DTXSID3063598

29171990

Characteristics

43.4

1.4

Clear Liquid

1.3±0.1 g/cm3

156-158 °C @ Solvent: Ethanol

137 °C

41 °C

1.425

Slightly miscible with water.

Flammables area

7.61 mmHg

Safety Information

8

2920

3

34-29-20/21/22-14-10-37-36

8-45-36/37/39-26-16

C,F

Stable under normal temperatures and pressures.

P280-P305 + P351 + P338-P310

H226-H314

|Danger|H226 (96.77%): Flammable liquid and vapor [Warning Flammable liquids]|P210, P233, P234, P240, P241, P242, P243, P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P330, P363, P370+P378, P390, P403+P233, P403+P235, P404, P405, and P501|Aggregated GHS information provided by 62 companies from 11 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

ethoxalyl chloride

Ethyl oxalyl chloride Use and Manufacturing

Methods of Manufacturing

A mixture of potassium acetate (20 g), water (30 ml) and diethyl oxalate (29.2 g, 0.2 mol) was stirred at 70-80 °C for 2 h. The reaction mixture was cooled and condensed to 30 ml. After ethanol (50 ml) and diethyl ether (150 ml) were added, the solution was filtrated to give 23.61 g of potassium monoethyl oxalate (76percent). SOCl

Uses

For organic synthesis

Acetic acid, 2-chloro-2-oxo-, ethyl ester: ACTIVE

Computed Properties

Molecular Weight:136.53
XLogP3:1.4
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:135.9927217
Monoisotopic Mass:135.9927217
Topological Polar Surface Area:43.4
Heavy Atom Count:8
Complexity:110
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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