CAS 638-07-3
:Ethyl 4-chloroacetoacetate
Description:
Ethyl 4-chloroacetoacetate is an organic compound characterized by its ester functional group and the presence of a chlorine atom. It is typically a colorless to pale yellow liquid with a fruity odor, indicating its volatility and potential for use in various chemical reactions. The compound features a 4-chloro substituent on the aromatic ring, which enhances its reactivity, making it useful in synthetic organic chemistry, particularly in the synthesis of pharmaceuticals and agrochemicals. Ethyl 4-chloroacetoacetate is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. It is known for its role as a building block in the synthesis of more complex molecules, often participating in nucleophilic substitution and condensation reactions. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate personal protective equipment should be used to minimize exposure.
Formula:C6H9ClO3
InChI:InChI=1S/C6H9ClO3/c1-2-10-6(9)3-5(8)4-7/h2-4H2,1H3
InChI key:InChIKey=OHLRLMWUFVDREV-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)C(CCl)=O
Synonyms:- 1-(5-Ethyl-2-Pyridyl)Ethane-1,2-Diol
- 4-Chloro acetoethylacetate
- 4-Chloro-3-Oxo-Butanoicaciethylester
- 4-Chloro-3-oxobutanoic acid ethyl ester
- 4-Chloro-3-oxobutyric acid ethyl ester
- 4-Chloro-Acetoaceticaciethylester
- 4-Chloroacetoacetate d'ethyle
- 4-Cloroacetoacetato De Etilo
- Acetoacetate, 4-Chloro-, Ethyl
- Acetoacetic acid, 4-chloro-, ethyl ester
- Butanoic Acid, 4-Chloro-3-Oxo-Ethyl Ester
- Ethyl (chloroacetyl)acetate
- Ethyl 3-oxo-4-chlorobutanoate
- Ethyl 4-Chloro Acetoacetate
- Ethyl 4-Chloroacetoacetate
- Ethyl 4-chloro-3-oxobutanoate
- Ethyl 4-chloro-3-oxobutyrate
- Ethyl chloroacetoacetate
- Ethyl γ-chloroacetoacetate
- Ethyl ω-chloroacetoacetate
- Ethyl-4-Chloro Aceto Acetate
- Ethyl-4-chloracetoacetat
- Ethyl-Gamma-Chloroacetoacetate
- See more synonyms
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Found 9 products.
Ethyl 4-chloroacetoacetate, 97%
CAS:Ethyl 4-chloroacetoacetate is used as a precursor in the preparation of phosphorous ylides. It finds application in regular film coating, pharmaceutical coating and formulation. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentationFormula:C6H9ClO3Purity:97%Color and Shape:Clear colorless to pale yellow, LiquidMolecular weight:164.59Ethyl 4-chloroacetoacetate
CAS:Formula:C6H9ClO3Purity:95%Color and Shape:LiquidMolecular weight:164.5869Ethyl 4-chloro-3-oxobutanoate
CAS:Ethyl 4-chloro-3-oxobutanoateFormula:C6H9ClO3Purity:97%Molecular weight:164.59Ethyl 4-chloroacetoacetate
CAS:Ethyl 4-chloroacetoacetateFormula:C6H9ClO3Purity:99%Color and Shape:Colourless Liquid-ClearMolecular weight:164.58686Ethyl 4-chloro-3-oxobutanoate
CAS:Formula:C6H9ClO3Purity:95%Color and Shape:Liquid, ClearMolecular weight:164.59Ethyl 4-Chloroacetoacetate
CAS:Controlled ProductApplications Ethyl 4-Chloroacetoacetate (cas# 638-07-3) is a compound useful in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the packageFormula:C6H9ClO3Color and Shape:NeatMolecular weight:164.59Ethyl 4-chloroacetoacetate
CAS:Ethyl 4-chloroacetoacetate is a chiral organic compound that is synthesized by the asymmetric synthesis of ethyl chloroacetate. This reaction is performed in an organic solution, using sodium salts as the solvent. The expression plasmid and logarithmic growth phase are needed for the enzyme catalysis and stereoselective reactions. The reaction solution is recombined with hydrochloric acid and chiral compound to produce high yields of ethyl 4-chloroacetoacetate.Formula:C6H9ClO3Purity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:164.59 g/molEthyl 4-Chloroacetoacetate
CAS:Formula:C6H9ClO3Purity:>95.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:164.59
