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Structure of 203314-33-4
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Methyl 2-(5-bromo-2-chlorophenyl)acetate features a bromo-chloro-substituted phenyl ring that confers enhanced electron-withdrawing character, enabling efficient coupling in cross-coupling reactions. The methyl ester group provides a stable, bench-ready handle for downstream functionalization, while the halogenated aromatic core supports selective transformations under palladium catalysis.
Methyl 2-(5-bromo-2-chlorophenyl)acetate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of biaryl scaffolds via palladium-catalyzed cross-coupling reactions. The ortho-halogenated aryl motif provides high regioselectivity in Suzuki, Stille, and Negishi couplings, while the ester group offers compatibility with subsequent transformations including hydrolysis, reduction, and nucleophilic substitution. Bench-stable and readily purified by flash chromatography, it facilitates scalable synthesis of complex heterocyclic and functionalized aromatic systems.
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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: