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Structure of 135613-33-1
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Ethyl 3-(2-bromophenyl)propanoate features a brominated phenyl ring positioned ortho to the propionate chain, enabling direct functionalization in cross-coupling reactions. This bench-stable ester integrates readily into synthetic sequences requiring aryl halide handles, delivering high yields under standard palladium-catalyzed conditions.
Ethyl 3-(2-bromophenyl)propanoate serves as a versatile building block in synthetic organic chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined aryl bromide functionality. The ester group offers compatibility with standard reductions and hydrolysis protocols, facilitating access to carboxylic acid derivatives. Its bench-stable nature and predictable reactivity make it suitable for iterative synthesis of complex scaffolds, including biaryl and heterocyclic systems common in medicinal chemistry workflows.
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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: