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Structure of 150812-32-1
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2-Amino-4-bromo-5-chlorobenzoic acid features a polar carboxylic acid group paired with electron-withdrawing bromo and chloro substituents, enabling selective coupling in heterocyclic synthesis. The amino functionality supports derivatization under mild conditions, while the halogenated aryl core enhances reactivity in transition metal-catalyzed transformations. This scaffold delivers precise structural control for advanced pharmaceutical intermediates.
2-Amino-4-bromo-5-chlorobenzoic acid serves as a versatile building block for pharmaceutical intermediates and agrochemical scaffolds. Its ortho-amino and carboxylic acid functionalities enable direct coupling reactions, while the bromo and chloro substituents support palladium-catalyzed cross-coupling transformations. The compound exhibits good bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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: