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Structure of 1515982-14-5
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5-Bromo-1-methyl-1H-pyrrole-3-carboxylic acid features a brominated pyrrole core with a methyl group at the nitrogen and a carboxylic acid at the 3-position, enabling direct incorporation into bioactive scaffolds. The electron-deficient pyrrole ring facilitates transition metal-catalyzed coupling reactions, while the carboxylic acid serves as a versatile handle for amide bond formation or derivatization. This compound offers enhanced stability and solubility in polar organic solvents, supporting efficient integration into medicinal chemistry campaigns.
5-Bromo-1-methyl-1H-pyrrole-3-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions at the bromo position. The carboxylic acid functionality facilitates derivatization via amide formation or esterification, while the methyl group enhances solubility and modulates electronic properties. Bench-stable and compatible with standard purification methods, it functions effectively in medicinal chemistry campaigns targeting pyrrole-based scaffolds.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362
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Lot numbers can be found on the outside label of a product: