CAS 609-15-4
:Éthyl 2-chloroacetoacétate
- 2-Chloro-3-oxobutanoic acid ethyl ester
- 2-Chloro-3-oxobutyric acid ethyl ester
- 2-Chloroacetoacetic acid ethyl ester
- A 21960
- Acetoacetic acid, 2-chloro-, ethyl ester
- Butanoic acid, 2-chloro-3-oxo-, ethyl ester
- Ethy 2-Chloroacetoacetate
- Ethyl 2-Chloro-3-Oxobutanoate
- Ethyl 2-chloracetoacetate
- Ethyl 2-chloro-3-oxobutyrate
- Ethyl α-chloroacetoacetate
- Ethyl α-chloroacetylacetate
- NSC 78426
- ethyl (2R)-2-chloro-3-oxobutanoate
- ethyl (2S)-2-chloro-3-oxobutanoate
- Ethyl-2-chloroacetoacetate
- Ethyl 2-chloroacetoacetate
- ETHYL ALPHA-CHLOROACETOACETATE
- ETHYL 2-CHLOROACETOACETATE, WACKERQUALIT Y
- Ethyl2-chloroacetoacetate,97%
- ETHYL CHLOROACETOACETATE
- 2-CL-ACE
- 2-CHLORACETYLETHYL ACETATE
- ETHYL A-CHLORO-ACETOACETATE
- ethyl2-chloroacettoacetate
- AKOS BBS-00004302
- A-CHLOROACETOACETIC ESTER
- 2-chloro-3-oxo-butanoicaciethylester
- Voir plus de synonymes
Ethyl 2-chloroacetoacetate, 96%
CAS :This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C6H9ClO3Degré de pureté :96%Couleur et forme :Clear, colourless to yellow, liquidMasse moléculaire :164.59Ethyl 2-chloroacetoacetate
CAS :Formule :C6H9ClO3Degré de pureté :95%Couleur et forme :LiquidMasse moléculaire :164.5869Ethyl 2-chloroacetoacetate
CAS :Formule :C6H9ClO3Degré de pureté :≥ 95.0%Couleur et forme :Clear, colourless to yellow liquidMasse moléculaire :164.59A 21960
CAS :A 21960, or Ethyl 2-chloroacetoacetate, blocks synapse formation and site-specific recombination, aiding in bacterial infection research.Formule :C6H9ClO3Degré de pureté :99.46%Couleur et forme :SolidMasse moléculaire :164.59Febuxostat Impurity 61
CAS :Formule :C6H9ClO3Couleur et forme :Colorless LiquidMasse moléculaire :164.59Ethyl 2-Chloroacetoacetate
CAS :Formule :C6H9ClO3Degré de pureté :>95.0%(GC)Couleur et forme :Colorless to Light orange to Yellow clear liquidMasse moléculaire :164.59Ethyl 2-chloroacetoacetate
CAS :Ethyl 2-chloroacetoacetateFormule :C6H9ClO3Degré de pureté :98%Couleur et forme : colourless liquidMasse moléculaire :164.58686g/molEthyl 2-Chloracetoacetate
CAS :Applications Ethyl 2-Chloracetoacetate is used in the preparation of oxazoles and thiazoles as agonists for peroxisome proliferator-activated receptor δ. It is also used to synthesize dimethylimidazothiadiazolecarbohydrazides with anticancer activities.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Sznaidman, M., et al.: Bioorg. Med. chem. Lett., 13, 1517 (2003); Terzioglu, N., et al.: Eur. J. Med. Chem., 38, 781 (2003)Formule :C6H9ClO3Couleur et forme :NeatMasse moléculaire :164.59Ethyl Chloroacetoacetate
CAS :Formule :C6H9ClO3Degré de pureté :95%Couleur et forme :ClearMasse moléculaire :164.59Ethyl 2-chloroacetoacetate
CAS :Ethyl 2-chloroacetoacetate is an organic compound that is prepared industrially by the chlorination of acetoacetic acid. It has been shown to have antimicrobial activity against human pathogens, such as Staphylococcus aureus and Escherichia coli. The kinetic constants for this reaction are pH dependent and depend on the ionic strength of the solution. Ethyl 2-chloroacetoacetate reacts with hydroxide to form ethyl chlorocarbonate, which is hydrolyzed to give carbon dioxide and hydrogen chloride. The hydrogen bonding interactions between these two molecules are important in the mechanism of this reaction. This reaction also generates a characteristic NMR spectrum in which six peaks can be seen. Ethyl 2-chloroacetoacetate is acidic and hemolytic when dissolved in water, but it does not react with trifluoroacetic acid or low energy radiation.Formule :C6H9ClO3Degré de pureté :Min. 95%Couleur et forme :Clear LiquidMasse moléculaire :164.59 g/mol










