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Structure of 445303-24-2
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This imidazole derivative features a brominated phenyl group at the 3-position and a carboxylic acid at the 4-position, enabling direct coupling in cross-coupling reactions. The electron-deficient imidazole core enhances reactivity in transition-metal catalyzed transformations, while the bench-stable structure facilitates handling under standard conditions.
1-(3-Bromophenyl)-1H-imidazole-4-carboxylic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The bromo substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates derivatization via amide formation or esterification. Its stability under standard bench conditions and compatibility with diverse reaction environments make it a practical choice for medicinal chemistry and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: