Ethyl 5-fluoro-3-pyridineacetate 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 fluoro substituent at the 5-position and an ethyl ester functional group attached to the 3-position of the pyridine ring. Its molecular formula typically includes carbon, hydrogen, nitrogen, and fluorine atoms, reflecting its structure. Ethyl 5-fluoro-3-pyridineacetate is often utilized in medicinal chemistry and pharmaceutical research due to its potential biological activity. The presence of the fluorine atom can enhance the compound's lipophilicity and metabolic stability, making it an interesting candidate for drug development. Additionally, the ester functional group may influence its reactivity and solubility in various solvents. As with many organic compounds, safety data should be consulted for handling and storage, as it may pose health risks if not managed properly. Overall, this compound exemplifies the diverse applications of fluorinated organic molecules in chemical synthesis and drug discovery.

Ethyl 5-fluoro-3-pyridineacetate

39891-14-0: (5-Fluoro-Pyridin-3-Yl)-Acetic Acid Ethyl Ester, 3-Pyridineacetic acid, 5-fluoro-, ethyl ester, 5-Fluor-3-pyridylessigsaeureethylester, Ethyl 2-(5-Fluoropyridin-3-Yl)Acetate, Ethyl 5-fluoro-3-pyridineacetate

CAS 39891-14-0: Ethyl 5-fluoro-3-pyridineacetate

Ethyl 2-(5-fluoropyridin-3-yl)acetate

Ref: 10-F364073

ethyl 2-(5-fluoropyridin-3-yl)acetate

Ref: IN-DA00CMOH

Ethyl 2-(5-fluoropyridin-3-yl)acetate

Ref: 54-PC905564