2-Fluoro-3-oxopentanoic acid ethyl ester, with the CAS number 759-67-1, is an organic compound characterized by its ester functional group and a fluorine atom substitution. This compound typically exhibits a moderate polarity due to the presence of both the ester and carboxylic acid functionalities, which can influence its solubility in various solvents. The presence of the fluorine atom can enhance its reactivity and may impart unique properties such as increased lipophilicity or altered biological activity. It is generally a colorless to pale yellow liquid with a characteristic odor. The compound is used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its reactivity can be attributed to the carbonyl group, making it susceptible to nucleophilic attack. Safety data should be consulted for handling, as it may pose health risks if inhaled or ingested. Overall, 2-fluoro-3-oxopentanoic acid ethyl ester is a versatile compound with applications in various chemical processes.

2-fluoro-3-oxopentanoic acid ethylester

759-67-1: 2-Fluoro-3-Oxo-Pentanoic Acid Ethyl Ester, Ethyl 2-Fluoro-3-Oxopentanoate, Ethyl2-fluoro-3-oxovalerate, Ethyl2-Fluoro-3-Oxopentanoa

Ethyl 2-fluoro-3-oxopentanoate

Voriconazole Impurity 39

Voriconazole Impurity 27

ETHYL 2-FLUORO-3-OXOPENTANOATE

Ethyl-2-fluoro-3-oxopentanoate is a byproduct of the reaction between formamide and propionyl chloride. It can be reacted with sodium hydrogen carbonate to produce ethyl 2-fluoro-3-oxopentanoate, which is a precursor to voriconazole.

CAS 759-67-1: 2-fluoro-3-oxopentanoic acid ethylester

Ethyl 2-fluoro-3-oxopentanoate

Ref: IN-DA005SPK

Voriconazole Impurity 39

Ref: ST-EA-CP-V13034

Voriconazole Impurity 27

Ref: 4Z-V-1049

ETHYL 2-FLUORO-3-OXOPENTANOATE

Ref: 10-F849424

Ethyl-2-fluoro-3-oxopentanoate

Ref: 3D-FE30115

Ethyl 2-fluoro-3-oxopentanoate

Ref: 54-PC902638