4-Pyridinepropanoic acid, ethyl ester, also known by its CAS number 52809-19-5, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a propanoic acid moiety, where the carboxylic acid group is esterified with an ethyl group, enhancing its solubility in organic solvents. It typically appears as a colorless to pale yellow liquid with a distinctive odor. The presence of the pyridine ring contributes to its basicity and potential reactivity, making it useful in various chemical syntheses and applications, including pharmaceuticals and agrochemicals. Its molecular structure allows for hydrogen bonding, influencing its physical properties such as boiling point and solubility. Additionally, 4-Pyridinepropanoic acid, ethyl ester may exhibit biological activity, which can be explored in medicinal chemistry. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.

4-Pyridinepropanoic acid, ethyl ester

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Ethyl 3-(4-Pyridyl)propanoate

Ethyl 3-(4-pyridyl)propanoate is an ancillary that is used in the formation of conjugates. It has a metal insertion mechanism, which inserts a metal atom into the organic molecule. The nitrogen atoms are positioned so they can form bonds to two other molecules. The molecule has a photophysical response pathway and luminescent properties. Ethyl 3-(4-pyridyl)propanoate may be used in cancer or sclerosis treatments, as it focuses on response pathways and also has photophysical properties.

CAS 52809-19-5: 4-Pyridinepropanoic acid, ethyl ester

Ethyl 3-(4-Pyridyl)propanoate

Ref: 54-OR470608

Ethyl 3-(4-Pyridyl)propanoate

Ref: 3D-CCA80919

Ethyl 3-(pyridin-4-yl)propanoate

Ref: 10-F756007

4-Pyridinepropanoic acid, ethyl ester

Ref: IN-DA00I9FW