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Structure of 188347-49-1
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This dibrominated phenylacetic acid features a sterically hindered aryl moiety with two bromine atoms positioned at the 3 and 5 ring positions, enhancing its utility in cross-coupling reactions. The carboxylic acid functional group enables direct derivatization or incorporation into pharmaceutical intermediates. Bench-stable and moisture-tolerant, it serves as a reliable building block for complex molecular architectures.
2-(3,5-Dibromophenyl)acetic acid serves as a versatile building block for brominated aromatic scaffolds in medicinal chemistry and materials science. Its dibromo substitution pattern enables selective cross-coupling reactions, while the acetic acid functionality facilitates derivatization via esterification or amidation. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for iterative synthetic workflows requiring halogen-directed functionalization.
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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: