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Structure of 152213-63-3
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Methyl 2-(6-bromo-1H-indol-3-yl)acetate features a brominated indole core with a pendant acetate ester, enabling direct functionalization in cross-coupling and bioconjugation workflows. The electron-deficient bromine at the C6 position facilitates palladium-catalyzed transformations, while the methyl ester serves as a handle for selective derivatization. This bench-stable compound integrates readily into complex heterocyclic architectures.
Methyl 2-(6-bromo-1H-indol-3-yl)acetate serves as a versatile building block for indole-based scaffolds, enabling efficient functionalization at the C3 position. The bromine substituent facilitates palladium-catalyzed cross-coupling reactions, while the ester group supports further derivatization via hydrolysis or reduction. Its bench-stable nature and compatibility with standard synthetic workflows make it ideal for medicinal chemistry campaigns targeting heterocyclic APIs.
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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: