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Structure of 400071-95-6
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5-Bromo-1-methyl-1H-indole-3-carboxylic acid features a brominated indole core with a methyl group at the nitrogen and a carboxylic acid at the 3-position, enabling direct integration into bioactive molecule scaffolds. The electron-withdrawing bromine enhances reactivity in cross-coupling processes, while the carboxylic acid provides a handle for derivatization under standard conditions.
5-Bromo-1-methyl-1H-indole-3-carboxylic acid serves as a versatile building block in medicinal chemistry, enabling direct incorporation into biologically active indole scaffolds. Its bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the carboxylic acid group supports amide formation and derivatization under standard conditions. The molecule exhibits excellent bench stability and is readily purified by crystallization, making it well-suited for scalable synthesis 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-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: