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Structure of 1260753-02-3
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5-Bromo-1H-imidazole-2-carboxylic acid features a brominated imidazole core with a carboxylic acid group at the 2-position, enabling direct conjugation or derivatization. The electron-withdrawing bromine enhances reactivity in cross-coupling processes, while the acidic proton facilitates salt formation and purification. This bench-stable, moisture-tolerant scaffold integrates efficiently into bioactive molecules and functional materials.
5-Bromo-1H-imidazole-2-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation of brominated imidazole motifs into bioactive scaffolds. Its carboxylic acid functionality facilitates amide bond formation and derivatization, while the bromine substituent supports palladium-catalyzed cross-coupling reactions. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis workflows 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: