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Structure of 1403457-00-0
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Methyl 7-bromo-1H-indole-6-carboxylate features a brominated indole scaffold with a strategically positioned ester group, enabling direct functionalization in transition-metal-catalyzed couplings. The electron-deficient indole core enhances reactivity in cross-coupling processes, while the methyl ester offers stability and compatibility with diverse reaction conditions. This compound serves as a key intermediate for synthesizing biologically active heterocycles and advanced pharmaceutical candidates.
Methyl 7-bromo-1H-indole-6-carboxylate serves as a versatile building block for the synthesis of substituted indoles and heterocyclic scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports selective transformations. Its bench-stable nature and compatibility with standard synthetic protocols facilitate efficient access to complex molecular architectures in medicinal chemistry and materials science.
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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: