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Structure of 58026-21-4
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2-Amino-5-bromo-3-chlorobenzoic acid features a highly functionalized aromatic core with complementary electron-donating and withdrawing substituents. This combination enables efficient coupling in cross-coupling reactions and facilitates integration into bioactive scaffolds requiring precise electronic tuning. The carboxylic acid group supports derivatization, while the amino functionality offers direct access to amide and heterocyclic linkages.
2-Amino-5-bromo-3-chlorobenzoic acid serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, offering orthogonal functional handles for downstream derivatization. The amino group enables nucleophilic substitution or coupling reactions, while the bromo and chloro substituents facilitate palladium-catalyzed cross-couplings. Its bench-stable crystalline form simplifies handling and purification, making it well-suited for modular synthesis of complex scaffolds in API 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: