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Structure of 22514-58-5
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2-Bromobenzo[d]thiazole-6-carboxylic acid features a fused heterocyclic core with a bromine atom at the benzo ring and a carboxylic acid group at the thiazole C6 position. This combination enables direct functionalization in cross-coupling reactions and facilitates conjugation to biomolecules or polymer backbones under standard conditions. The molecule exhibits good stability and solubility in polar organic solvents, supporting its use in synthetic chemistry workflows.
2-Bromobenzo[d]thiazole-6-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions at the bromine site. The carboxylic acid functionality provides a handle for derivatization via amide bond formation or esterification, supporting modular scaffold development. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate synthesis.
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Lot numbers can be found on the outside label of a product: