Ethyl 3-oxopropanoate, also known as ethyl acetoacetate, is an organic compound characterized by its ester functional group and a ketone moiety. It typically appears as a colorless to pale yellow liquid with a fruity odor. This compound is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. Ethyl 3-oxopropanoate is known for its reactivity in various chemical reactions, including Claisen condensation and Michael addition, making it a valuable intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and flavoring agents. Its molecular structure features a five-membered carbon chain with a carbonyl group, contributing to its chemical reactivity. Additionally, it has a moderate boiling point and a relatively low flash point, indicating that it should be handled with care in laboratory settings. Overall, ethyl 3-oxopropanoate is an important compound in synthetic organic chemistry due to its versatility and reactivity.

ethyl 3-oxopropanoate

34780-29-5: Ethyl 3-oxopropanoate, also known as ethyl acetoacetate, is an organic compound characterized by its ester functional group and a ketone moiety. It typically appears as a colorless to pale yellow liquid with a fruity odor. This compound is soluble in organic solvents such as ethanol and ether but has limited solubility in water due to its hydrophobic nature. Ethyl 3-oxopropanoate is known for its reactivity in various chemical reactions, including Claisen condensation and Michael addition, making it a valuable intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and flavoring agents. Its molecular structure features a five-membered carbon chain with a carbonyl group, contributing to its chemical reactivity. Additionally, it has a moderate boiling point and a relatively low flash point, indicating that it should be handled with care in laboratory settings. Overall, ethyl 3-oxopropanoate is an important compound in synthetic organic chemistry due to its versatility and reactivity.

CAS 34780-29-5

ethyl 3-oxopropanoate

3-Oxopropionic acid ethyl ester

Ref: IN-DA0037C0

Regadenoson Impurity 56

Ref: 4Z-R-095058