CAS 607-97-6
:Ethyl 2-ethylacetoacetate
Description:
Ethyl 2-ethylacetoacetate, with the CAS number 607-97-6, is an organic compound that belongs to the class of β-keto esters. It is characterized by its ethyl ester functional group and a 2-ethyl substituent on the acetoacetate moiety. This compound typically appears as a colorless to pale yellow liquid with a fruity odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. Ethyl 2-ethylacetoacetate is known for its reactivity, particularly in condensation reactions, making it useful in organic synthesis, including the preparation of various pharmaceuticals and agrochemicals. Additionally, it can undergo enolization, which is significant in its chemical behavior and reactivity. Safety data indicates that it should be handled with care, as it may cause irritation to the skin and eyes. Overall, its unique structure and reactivity make it a valuable compound in synthetic organic chemistry.
Formula:C8H14O3
InChI:InChI=1S/C8H14O3/c1-4-7(6(3)9)8(10)11-5-2/h7H,4-5H2,1-3H3
InChI key:InChIKey=OKANYBNORCUPKZ-UHFFFAOYSA-N
SMILES:C(C(OCC)=O)(C(C)=O)CC
Synonyms:- 2-Ethyl-3-oxo-butyric acid ethyl ester
- 2-Ethyl-3-oxobutanoic acid ethyl ester
- 2-Ethylacetoacetic acid ethyl ester
- Acetoacetic acid, 2-ethyl-, ethyl ester
- Butanoic acid, 2-ethyl-3-oxo-, ethyl ester
- Ethyl 2-acetylbutanoate
- Ethyl 2-acetylbutyrate
- Ethyl 2-ethyl-3-ketobutyrate
- Ethyl 2-ethyl-3-oxobutanoate
- Ethyl 2-ethyl-3-oxobutanoate:Diethyl acetoacetate
- Ethyl 2-ethyl-3-oxobutyrate
- Ethyl 2-ethylacetylacetate
- Ethyl α-acetylbutyrate
- Ethyl α-ethylacetoacetate
- NSC 53775
- ethyl (2R)-2-ethyl-3-oxobutanoate
- See more synonyms
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Found 10 products.
Ethyl 2-Ethylacetoacetate
CAS:Formula:C8H14O3Purity:>97.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:158.20Ethyl 2-ethylacetoacetate, 95%
CAS:<p>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</p>Formula:C8H14O3Purity:95%Color and Shape:Liquid, Clear colorlessMolecular weight:158.20Ethyl 2-ethyl-3-oxobutanoate
CAS:Formula:C8H14O3Purity:98%Color and Shape:LiquidMolecular weight:158.1950Ethyl 2-ethylacetoacetate
CAS:<p>Ethyl 2-ethylacetoacetate</p>Purity:97%Color and Shape:LiquidMolecular weight:158.19g/molRef: 54-OR905609
10lTo inquire5mlTo inquire100gTo inquire2.5lTo inquire25mlTo inquire500gTo inquire100mlTo inquire500mlTo inquireEthyl 2-ethylacetoacetate
CAS:Formula:C8H14O3Purity:95%Color and Shape:LiquidMolecular weight:158.197Ethyl 2-Ethylacetoacetate
CAS:Controlled Product<p>Applications Ethyl 2-Ethylacetoacetate was a useful reagent in systematic investigation of saccharomyces cerevisiae enzymes catalyzing carbonyl reductions.<br>References Kaluzna, I., et al.: J. Am. Chem. Soc., 126, 12827 (2004);<br></p>Formula:C8H14O3Color and Shape:NeatMolecular weight:158.19Ethyl 2-ethylacetoacetate
CAS:<p>Ethyl 2-ethylacetoacetate is a carbonyl compound that belongs to the supramolecular class of chromenones. The molecule has an x-ray diffraction pattern that is characteristic of a ring structure. It can be synthesized by an efficient method involving the reaction of ethyl benzoylacetate with a halide in the presence of acid catalyst. The reactants are isolated in high yield and structural analysis shows the presence of a methylene group and an ethyl group on opposite sides of the ring, which are bonded to each other through an acetoacetate group. This chromenone also displays photochemical properties and can be used as a substrate for functional theory studies.</p>Formula:C8H14O3Purity:Min. 95%Molecular weight:158.19 g/mol
