Uses
ChemicalBook > CAS DataBase List > Ethyl chlorooxoacetate

Ethyl chlorooxoacetate

Uses
Product Name
Ethyl chlorooxoacetate
CAS No.
4755-77-5
Chemical Name
Ethyl chlorooxoacetate
Synonyms
Ethyl 2-chloro-2-oxoacetate;ETHYL OXALYL CHLORIDE;ETHYL CHLOROOXOACETATE;ETHYL CHLOROGLYOXYLATE;ETHOXALYL CHLORIDE;ETCOX;2-chloro-2-oxoacetate;mono-Ethyl oxalyl chloride;Ethyl (Chlorocarbonyl)formate;orooxoacetate
CBNumber
CB1257382
Molecular Formula
C4H5ClO3
Formula Weight
136.53
MOL File
4755-77-5.mol
More
Less

Ethyl chlorooxoacetate Property

Melting point:
156-158 °C(Solv: ethanol (64-17-5))
Boiling point:
135 °C
Density 
1.222 g/mL at 25 °C(lit.)
refractive index 
1.416-1.418
Flash point:
41 °C
storage temp. 
Inert atmosphere,2-8°C
solubility 
soluble in Chloroform
form 
Liquid
color 
Clear
Specific Gravity
1.222
Water Solubility 
Slightly miscible with water.
Sensitive 
Moisture Sensitive
BRN 
506725
InChIKey
OWZFULPEVHKEKS-UHFFFAOYSA-N
CAS DataBase Reference
4755-77-5(CAS DataBase Reference)
NIST Chemistry Reference
Chlorooxalic acid, ethyl ester(4755-77-5)
EPA Substance Registry System
Acetic acid, chlorooxo-, ethyl ester (4755-77-5)
More
Less

Safety

Hazard Codes 
C,F
Risk Statements 
34-29-20/21/22-14-10-37-36
Safety Statements 
8-45-36/37/39-26-16
RIDADR 
2920
WGK Germany 
3
TSCA 
Yes
HazardClass 
8
PackingGroup 
II
HS Code 
29171990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H226Flammable liquid and vapour

H314Causes severe skin burns and eye damage

H335May cause respiratory irritation

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P303+P361+P353IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
E43101
Product name
Ethyl chlorooxoacetate
Purity
98%
Packaging
25g
Price
$46.8
Updated
2025/07/31
Sigma-Aldrich
Product number
E43101
Product name
Ethyl chlorooxoacetate
Purity
98%
Packaging
100g
Price
$103
Updated
2025/07/31
TCI Chemical
Product number
C1066
Product name
Ethyl Chloroglyoxylate
Purity
>98.0%(T)
Packaging
25g
Price
$73
Updated
2025/07/31
TCI Chemical
Product number
C1066
Product name
Ethyl Chloroglyoxylate
Purity
>98.0%(T)
Packaging
100g
Price
$192
Updated
2025/07/31
Sigma-Aldrich
Product number
E43101
Product name
Ethyl chlorooxoacetate
Purity
98%
Packaging
500g
Price
$141
Updated
2025/07/31
More
Less

Ethyl chlorooxoacetate Chemical Properties,Usage,Production

Uses

Ethyl oxalyl monochloride is used in the synthesis of 2-oxo-3-alkenoic esters and alpha-keto ester in good yield. Ethyl oxalyl monochloride acts as a reactant in the preparation of oxyoxalamide derivatives as an epoxide hydrolase inhibitor.

Description

Ethyl chlorooxoacetate has been used as a reactant in the preparation of oxyoxalamide derivatives as epoxide hydrolase inhibitors.

Chemical Properties

clear liquid

Uses

Ethyl oxalyl chloride is used in the synthesis of 2-oxo-3-alkenoic esters and alpha-keto ester in good yield. It acts as a reactant in the preparation of oxyoxalamide derivatives as an epoxide hydrolase inhibitor.

Uses

Ethyl chlorooxoacetate can be used for the synthesis of:

  • α-keto esters.
  • Functionalized 3-pyrolin-2-ones.
  • Substituted arylglyoxylic acids via Friedel–Crafts acylation.
  • Substituted 9,10-phenanthrenequinones.
  • Quinoxalinone derivatives.

reaction suitability

reagent type: oxidant

Synthesis

95-92-1

4755-77-5

The general procedure for the synthesis of monoethyl oxalyl chloride from diethyl oxalate was as follows: a mixture of potassium acetate (20 g), water (30 mL) and diethyl oxalate (29.2 g, 0.2 mol) was stirred and reacted for 2 hours at 70-80 °C. Upon completion of the reaction, the reaction mixture was cooled and concentrated to 30 mL. Subsequently, ethanol (50 mL) and ether (150 mL) were added and the mixed solution was filtered to afford 23.61 g of potassium monoethyl oxalate (76% yield). The dried potassium monoethyl oxalate (20.6 g, 0.13 mol) was pre-mixed with diethyl ether (20 mL) in an ice bath and SOCl2 (30 g, 0.25 mol) was added slowly. The reaction mixture was heated under reflux conditions for 15 hours. At the end of the reaction, the resulting white solid of potassium chloride was removed by filtration, the filtrate was separated and the 125-130 °C fraction was collected by distillation to give 12.22 g of monoethyl oxalyl chloride (69% yield).

References

[1] Gazzetta Chimica Italiana, 1891, vol. 21 I, p. 306
[2] Monatshefte fuer Chemie, 1905, vol. 26, p. 375
[3] Chemische Berichte, 1886, vol. 19, p. 2159
[4] Justus Liebigs Annalen der Chemie, 1889, vol. 254, p. 27
[5] Recueil des Travaux Chimiques des Pays-Bas, 1907, vol. 26, p. 381

Ethyl chlorooxoacetate Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Ethyl chlorooxoacetate Suppliers

Bide Pharmatech Ltd.
Tel
400-6005915
Email
sales@picasso-e.com
Country
China
ProdList
39665
Advantage
58
Jiaxing Zhejia Biotechnology Co., LTD
Tel
0573-85609002 18367600069;
Email
zhejia01@163.com
Country
China
ProdList
8886
Advantage
58
Shandong Jiuyue Biological Technology Co. LT
Tel
18853316981
Email
1214127295@qq.com
Country
China
ProdList
132
Advantage
58
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
4006356688 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40228
Advantage
62
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15838
Advantage
69
Alfa Aesar
Tel
400-6106006
Fax
021-67582001/03/05
Email
saleschina@alfa-asia.com
Country
China
ProdList
30123
Advantage
84
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24529
Advantage
81
Beijing dtftchem Technology Co., Ltd.
Tel
010-60275820 13031183356
Fax
010-60270825
Email
elainezt@sina.com
Country
China
ProdList
1390
Advantage
62
Beijing HwrkChemical Technology Co., Ltd
Tel
18515581800 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
9400
Advantage
55
More
Less

View Lastest Price from Ethyl chlorooxoacetate manufacturers

Shaanxi Dideu Medichem Co. Ltd
Product
Ethyl oxalyl monochloride 4755-77-5
Price
US $1.00-1.50/KG
Min. Order
1KG
Purity
99%
Supply Ability
100000KG
Release date
2024-08-16
Henan Fengda Chemical Co., Ltd
Product
Ethyl oxalyl monochloride 4755-77-5
Price
US $8.00-0.80/KG
Min. Order
1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2024-01-22
Hangzhou ICH Biofarm Co., Ltd
Product
Ethyl oxalyl monochloride 4755-77-5
Price
US $0.00/kg
Min. Order
1kg
Purity
99.0%min
Supply Ability
10000kg
Release date
2023-06-09

4755-77-5, Ethyl chlorooxoacetateRelated Search:


  • ETHOXALYL CHLORIDE
  • ETCOX
  • Monoethyl oxalyl chloride
  • mono-Ethyl oxalyl chloride
  • Ethyl chloroglyoxylate~Oxalic acid monoethyl ester chloride
  • ETHYL CHLOROOXOACETATE,98%
  • Ethyloxalylchloride,98%
  • 2-chloro-2-oxoacetate
  • Ethyl (Chlorocarbonyl)formate
  • Ethyl chloroglyoxylate, mono-Ethyl oxalyl chloride, Monoethyl oxalyl chloride, Oxalic acid monoethyl ester chloride
  • Ethyl chloroglyoxylate, Monoethyl oxalyl chloride, Oxalic acid monoethyl ester chloride
  • 2-Oxo-2-chloroacetic acid ethyl ester
  • Chloroformylformic acid ethyl
  • Ethyl chlorooxoacetate,Ethyl chloroglyoxylate, Monoethyl oxalyl chloride, Oxalic acid monoethyl ester chloride, mono-Ethyl oxalyl chloride
  • Ethylestertwochloride
  • Ethyl chloride single grass
  • Ethyl oxalyl chloride, 98% 100ML
  • Ethyl oxalyl chloride, 98% 25ML
  • Acetic acid, 2-chloro-2-oxo-, ethyl ester
  • Chloroglyoxylic Acid Ethyl Ester Ethyl Chlorooxoacetate Ethyl Oxalyl Chloride Oxalic Acid Monoethyl Ester Chloride
  • Ethyl chlorooxoacetat
  • ETHYL OXALYL CHLORIDE
  • Ethyl oxalyl monochloride
  • ETHYL (CHLOROFORMYL)FORMATE
  • ETHYL CHLOROGLYOXALATE
  • ETHYL CHLOROGLYOXYLATE
  • ETHYL CHLOROOXOACETATE
  • CHLOROGLYOXYLIC ACID ETHYL ESTER
  • CHLOROFORMYLFORMIC ACID ETHYL ESTER
  • chlorooxalic acid ethyl ester
  • OXALIC ACID MONOETHYL ESTER CHLORIDE
  • Acetic acid, chlorooxo-, ethyl ester
  • chloro-oxo-aceticacidethylester
  • chlorooxo-aceticaciethylester
  • Ethoxy oxalylchloride
  • Ethyl 2-chloro-2-oxoacetate
  • Glyoxylic acid, chloro-, ethyl ester
  • Monoethyl oxaloyl chloride
  • oxalicacidethylesterchloride
  • Oxalyl chloride, ethyl ester
  • ethyleoxalyl chloride
  • Ethyl chloroglyoxylate mono-Ethyl oxalyl chloride Monoethyl oxalyl chloride Oxalic acid monoethyl ester chloride Chloroglyoxylic Acid Ethyl Ester Ethyl Oxalyl Chloride
  • Ethyl chloroformylformate for synthesis
  • orooxoacetate
  • Ethyl (Chlorocar
  • JACS-4755-77-5
  • Ethyl Chloroglyoxylate &gt
  • Ethyl Chloroglyoxalate,98%
  • Ethylchlorglyoxylat
  • ETHYL OXALYL1HLORIDE
  • Oxaloyl chloride monoethyl ester
  • Ethyl Oxalyl Chloride or Ethyl chloro oxo acetate
  • Ethyl chloroglyoxylateEthyl oxalyl monochloride
  • ETHLY CHLOROOXOACETATE
  • Ethyl oxalyl chloride 99%
  • 4755-77-5
  • ClCOCO2CH2CH3
  • ClCOCOOCH2CH3