Ethyl 2-(5-fluoro-2-methoxy-phenyl)-2-oxo-acetate, identified by its CAS number 873548-10-8, is an organic compound characterized by its ester functional group and a substituted aromatic ring. The presence of a fluorine atom and a methoxy group on the phenyl ring contributes to its unique chemical properties, including potential variations in reactivity and solubility. The compound features a carbonyl group (C=O) adjacent to the ester functionality, which can influence its reactivity in various chemical reactions, such as nucleophilic attacks. Ethyl 2-(5-fluoro-2-methoxy-phenyl)-2-oxo-acetate may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in synthesizing more complex molecules or as an intermediate in organic synthesis. Additionally, the presence of the fluorine atom can enhance lipophilicity, potentially affecting the compound's pharmacokinetic properties. Overall, this compound represents a versatile building block in organic synthesis with implications in various fields, including pharmaceuticals and agrochemicals.

ethyl 2-(5-fluoro-2-methoxy-phenyl)-2-oxo-acetate

873548-10-8: Ethyl 2-(5-fluoro-2-methoxy-phenyl)-2-oxo-acetate, identified by its CAS number 873548-10-8, is an organic compound characterized by its ester functional group and a substituted aromatic ring. The presence of a fluorine atom and a methoxy group on the phenyl ring contributes to its unique chemical properties, including potential variations in reactivity and solubility. The compound features a carbonyl group (C=O) adjacent to the ester functionality, which can influence its reactivity in various chemical reactions, such as nucleophilic attacks. Ethyl 2-(5-fluoro-2-methoxy-phenyl)-2-oxo-acetate may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its molecular structure suggests potential applications in synthesizing more complex molecules or as an intermediate in organic synthesis. Additionally, the presence of the fluorine atom can enhance lipophilicity, potentially affecting the compound's pharmacokinetic properties. Overall, this compound represents a versatile building block in organic synthesis with implications in various fields, including pharmaceuticals and agrochemicals.

CAS 873548-10-8

ethyl 2-(5-fluoro-2-methoxy-phenyl)-2-oxo-acetate

Ethyl 5-fluoro-2-methoxybenzoylformate

Ref: IN-DA008E5P

Ethyl 5-fluoro-2-methoxybenzoylformate

Ref: 54-PC1002523

Ethyl 5-fluoro-2-methoxybenzoylformate

Ref: 10-F201011