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Structure of 849934-94-7
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Methyl 2-(4-bromo-2-chlorophenyl)acetate features a sterically hindered aryl core with complementary halogen substituents, enabling selective cross-coupling reactions. The ester functionality provides enhanced solubility and stability under standard conditions, facilitating efficient integration into complex synthetic sequences.
Methyl 2-(4-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. Its orthogonal halogenation pattern supports sequential functionalization, while the ester group facilitates downstream transformations including hydrolysis, reduction, or amide formation. Bench-stable and readily purified by column chromatography, it functions reliably in multi-step syntheses requiring precise regiocontrol and functional group compatibility.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: