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Structure of 1021089-12-2
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Methyl 2-(2-bromo-3-chlorophenyl)acetate features a sterically accessible aryl core with orthogonal halogen handles, enabling sequential cross-coupling transformations. This bench-stable ester integrates readily into synthetic sequences requiring dual functionalization, delivering high chemoselectivity in palladium-catalyzed reactions under standard conditions.
Methyl 2-(2-bromo-3-chlorophenyl)acetate serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling efficient construction of substituted benzene scaffolds. Its ortho-bromo and meta-chloro substituents provide orthogonal reactivity for palladium-catalyzed cross-coupling and electrophilic substitution. The ester functionality facilitates further manipulation via hydrolysis or reduction, while the molecule exhibits good bench stability and ease of purification in standard synthetic workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: