Ethyl 3-(2-furyl)-3-oxopropanoate, with the CAS number 615-09-8, is an organic compound characterized by its ester functional group and a furan ring. This compound typically appears as a colorless to pale yellow liquid with a pleasant, fruity odor. It is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic furan moiety. The presence of the furan ring contributes to its aromatic properties, making it of interest in various chemical reactions, including those involving electrophilic substitution. Ethyl 3-(2-furyl)-3-oxopropanoate can participate in condensation reactions and is often utilized in the synthesis of more complex organic molecules. Its reactivity is influenced by the carbonyl group adjacent to the furan, which can engage in nucleophilic attacks. This compound is studied for its potential applications in pharmaceuticals, agrochemicals, and as a building block in organic synthesis. Proper handling and storage are essential due to its chemical properties and potential reactivity.

ethyl 3-(2-furyl)-3-oxopropanoate

615-09-8: Ethyl 3-Furan-2-Yl-3-Oxopropanoate

3-Furan-2-yl-3-oxo-propionic acid ethyl ester

Ethyl 3-(furan-2-yl)-3-oxopropanoate

Ethyl 3-(fur-2-yl)-3-oxopropanoate

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CAS 615-09-8: ethyl 3-(2-furyl)-3-oxopropanoate

3-Furan-2-yl-3-oxo-propionic acid ethyl ester

Ref: 10-F014827

Ethyl 3-(furan-2-yl)-3-oxopropanoate

Ref: IN-DA0034UP

Ethyl 3-(fur-2-yl)-3-oxopropanoate

Ref: 54-OR29821

Ethyl 3-furan-2-yl-3-oxo-propionate

Ref: 3D-FE50805