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Structure of 89245-41-0
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4-Bromoindole-3-acetic acid integrates a brominated indole ring with a carboxylic acid side chain, enabling direct functionalization in synthetic biology and medicinal chemistry workflows. This bench-stable derivative offers enhanced reactivity for coupling reactions and serves as a key building block in the development of bioactive molecules.
4-Bromoindole-3-acetic acid serves as a versatile building block in the synthesis of biologically active indole derivatives, particularly for constructing hormone analogs and heterocyclic scaffolds. Its bromine substituent enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid group facilitates direct amidation or esterification. The molecule exhibits good bench stability and is compatible with standard purification methods, making it suitable for iterative synthetic workflows in medicinal chemistry and natural product synthesis.
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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: