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Structure of 255064-08-5
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6-Bromo-1H-benzo[d]imidazole-4-carboxylic acid features a brominated imidazole core with a carboxylic acid handle at the 4-position, enabling direct conjugation in synthetic workflows. The electron-deficient heterocycle facilitates palladium-catalyzed coupling reactions, while the bench-stable functionality supports modular diversification in medicinal chemistry and materials synthesis.
6-Bromo-1H-benzo[d]imidazole-4-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined bromine handle and carboxylic acid functionality. The molecule exhibits bench stability and facilitates efficient derivatization in medicinal chemistry workflows, particularly in the construction of biologically relevant imidazole-based scaffolds. Its orthogonal reactivity supports modular functionalization under standard conditions.
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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: