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Structure of 54367-67-8
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5-Bromo-1-methyl-1H-pyrazole-4-carboxylic acid features a brominated pyrazole core with a methyl group at N1 and a carboxylic acid at C4, delivering enhanced electrophilicity for cross-coupling reactions. This bench-stable, moisture-tolerant reagent integrates readily into medicinal chemistry scaffolds and enables efficient access to bioactive heterocycles under standard conditions.
5-Bromo-1-methyl-1H-pyrazole-4-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling efficient access to functionalized pyrazole scaffolds. The molecule combines a bromine handle for palladium-catalyzed cross-coupling with a carboxylic acid group amenable to amidation or esterification, offering orthogonal reactivity for diversification. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for modular synthesis of bioactive compounds and API intermediates.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: