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Structure of 57699-28-2
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Methyl 2-(4-bromophenyl)-2-oxoacetate features a brominated aromatic ring coupled to a β-keto ester moiety, enabling direct functionalization in cross-coupling and heterocycle synthesis. The electron-deficient aryl group enhances reactivity in palladium-catalyzed transformations, while the ester functionality supports further derivatization under mild conditions. This compound serves as a key building block for pharmaceutical intermediates and advanced materials.
Methyl 2-(4-bromophenyl)-2-oxoacetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted benzophenones and heterocyclic scaffolds. Its brominated aryl group facilitates palladium-catalyzed cross-coupling reactions, while the α-keto ester functionality supports nucleophilic additions and condensation processes. The compound exhibits good bench stability and ease of purification, making it well-suited for iterative synthesis and scale-up applications in medicinal chemistry and process development.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: