CAS 609-15-4

Etil 2-cloroacetoacetato

Descrição:

Etil 2-cloroacetoacetato, com o número CAS 609-15-4, é um composto orgânico que pertence à classe dos acetoacetatos. É caracterizado pela presença de um éster etílico e um substituinte cloro na parte do acetoacetato. Este composto geralmente aparece como um líquido incolor a amarelo pálido com um odor frutado. É solúvel em solventes orgânicos como etanol e éter, mas tem solubilidade limitada em água devido ao seu grupo etílico hidrofóbico. Etil 2-cloroacetoacetato é conhecido por sua reatividade, particularmente em reações de substituição nucleofílica e condensação, tornando-se um intermediário valioso na síntese orgânica, especialmente na preparação de vários fármacos e agroquímicos. Além disso, pode sofrer hidrólise para formar o ácido e o álcool correspondentes. Devem ser tomadas precauções de segurança ao manusear este composto, pois pode representar riscos à saúde se inalado ou ingerido, e deve-se usar o equipamento de proteção adequado.

Fórmula: C₆H₉ClO₃

InChI: InChI=1/C6H9ClO3/c1-3-10-6(9)5(7)4(2)8/h5H,3H2,1-2H3/t5-/m1/s1

Chave InChI: InChIKey=RDULEYWUGKOCMR-UHFFFAOYSA-N

SMILES: C(C(OCC)=O)(C(C)=O)Cl

Sinónimos:

• 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

Ethyl 2-chloroacetoacetate, 96%

CAS: 609-15-4

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Fórmula: C₆H₉ClO₃

Pureza: 96%

Cor e Forma: Clear, colourless to yellow, liquid

Peso molecular: 164.59

Ref: 02-A19810

Ethyl 2-chloroacetoacetate

CAS: 609-15-4

Fórmula: C₆H₉ClO₃

Pureza: 95%

Cor e Forma: Liquid

Peso molecular: 164.5869

Ref: IN-DA0034UI

Ethyl 2-chloroacetoacetate

CAS: 609-15-4

Fórmula: C₆H₉ClO₃

Pureza: ≥ 95.0%

Cor e Forma: Clear, colourless to yellow liquid

Peso molecular: 164.59

Ref: 7W-GK6552

A 21960

CAS: 609-15-4

A 21960

Pureza: ≥98%

Peso molecular: 164.59g/mol

Ref: 54-BUP19427

A 21960

CAS: 609-15-4

A 21960, or Ethyl 2-chloroacetoacetate, blocks synapse formation and site-specific recombination, aiding in bacterial infection research.

Fórmula: C₆H₉ClO₃

Pureza: 99.46%

Cor e Forma: Solid

Peso molecular: 164.59

Ref: TM-T26408

Febuxostat Impurity 61

CAS: 609-15-4

Fórmula: C₆H₉ClO₃

Cor e Forma: Colorless Liquid

Peso molecular: 164.59

Ref: 4Z-F-3973

Ethyl 2-Chloroacetoacetate

CAS: 609-15-4

Fórmula: C₆H₉ClO₃

Pureza: >95.0%(GC)

Cor e Forma: Colorless to Light orange to Yellow clear liquid

Peso molecular: 164.59

Ref: 3B-C1218

Ethyl 2-chloroacetoacetate

CAS: 609-15-4

Ethyl 2-chloroacetoacetate

Fórmula: C₆H₉ClO₃

Pureza: 98%

Cor e Forma: colourless liquid

Peso molecular: 164.58686g/mol

Ref: 54-OR5481

Ethyl 2-Chloracetoacetate

CAS: 609-15-4

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)

Fórmula: C₆H₉ClO₃

Cor e Forma: Neat

Peso molecular: 164.59

Ref: TR-E903485

Ethyl Chloroacetoacetate

CAS: 609-15-4

Fórmula: C₆H₉ClO₃

Pureza: 95%

Cor e Forma: Clear

Peso molecular: 164.59

Ref: 10-F069254

Ethyl 2-chloroacetoacetate

CAS: 609-15-4

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.

Fórmula: C₆H₉ClO₃

Pureza: Min. 95%

Cor e Forma: Clear Liquid

Peso molecular: 164.59 g/mol

Ref: 3D-FE36663

Ethyl 2-Chloracetoacetate

CAS: 609-15-4

Fórmula: C₆H₉ClO₃

Peso molecular: 164.59

Ref: ST-EA-CP-F7031