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Structure of 152213-66-6
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This indole-based acetic acid derivative features a brominated indole core linked to a carboxylic acid side chain, enabling direct incorporation into bioconjugation workflows. The electron-deficient bromo-substituted ring enhances reactivity in cross-coupling reactions, while the pendant acid group facilitates derivatization via amide or ester formation under standard conditions.
2-(6-Bromo-1H-indol-3-yl)acetic acid serves as a versatile building block for the synthesis of indole-based pharmaceuticals and bioactive heterocycles. Its brominated indole moiety enables facile late-stage functionalization via palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates direct derivatization or incorporation into peptide-like scaffolds. The compound exhibits excellent bench stability and compatibility with standard purification methods, making it well-suited for iterative synthetic campaigns in medicinal chemistry and process development.
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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: