Ethyl 2-(5-bromobenzofuran-3-yl)acetate is an organic compound characterized by its ester functional group, which is derived from the reaction of ethyl alcohol and a carboxylic acid. This compound features a benzofuran moiety, specifically substituted with a bromine atom at the 5-position, which contributes to its unique chemical properties and potential biological activity. The presence of the ethyl acetate group suggests that it may exhibit moderate polarity, making it soluble in organic solvents while having limited solubility in water. The bromine substitution can enhance the compound's reactivity and may influence its interactions in various chemical environments. Ethyl 2-(5-bromobenzofuran-3-yl)acetate may be of interest in medicinal chemistry and materials science due to its structural features, which could lead to applications in drug development or as a building block in organic synthesis. As with many brominated compounds, considerations regarding environmental impact and safety are important, particularly in terms of toxicity and bioaccumulation.

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

200204-85-9: 3-Benzofuranacetic acid, 5-bromo-, ethyl ester, Ethyl (5-bromo-1-benzofuran-3-yl)acetate

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

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CAS 200204-85-9: ethyl 2-(5-bromobenzofuran-3-yl)acetate

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

Ref: 10-F093210

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

Ref: 3D-FE42053

3-Benzofuranacetic acid, 5-bromo-, ethyl ester

Ref: IN-DA002CMJ