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Structure of 63352-97-6
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This indole-acetic acid derivative features a brominated indole core linked to a carboxylic acid side chain, enabling direct integration into bioconjugation and medicinal chemistry workflows. The electron-deficient bromo substituent enhances reactivity in cross-coupling reactions, while the pendant acid group offers versatile derivatization potential for peptide and polymer conjugates under standard conditions.
2-(7-Bromo-1H-indol-3-yl)acetic acid serves as a versatile building block for indole-based bioactive molecules, enabling efficient access to pharmaceutically relevant scaffolds. The bromo substituent facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid group supports direct derivatization or incorporation into peptide-like systems. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for medicinal chemistry campaigns and process 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: