Ethyl 3-(2-bromophenyl)-3-oxopropanoate

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Reagent Code: #36418
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CAS Number 50671-05-1

science Other reagents with same CAS 50671-05-1

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Weight 271.1072 g/mol
Formula C₁₁H₁₁BrO₃
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MDL Number MFCD03424813
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Ethyl 3-(2-bromophenyl)-3-oxopropanoate is primarily used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and fine chemicals. Its structure, featuring a bromophenyl group and a β-keto ester moiety, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the development of compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are important in medicinal chemistry. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures.

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inventory 100mg
10-20 days ฿882.00

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Ethyl 3-(2-bromophenyl)-3-oxopropanoate
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Ethyl 3-(2-bromophenyl)-3-oxopropanoate is primarily used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and fine chemicals. Its structure, featuring a bromophenyl group and a β-keto ester moiety, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the development of compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it serves as a precursor in

Ethyl 3-(2-bromophenyl)-3-oxopropanoate is primarily used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and fine chemicals. Its structure, featuring a bromophenyl group and a β-keto ester moiety, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the development of compounds with potential biological activity, such as anti-inflammatory, antimicrobial, or anticancer agents. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are important in medicinal chemistry. The bromine atom in the molecule allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures.

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