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Structure of 91348-45-7
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Ethyl 3-bromo-1H-indole-2-carboxylate features a brominated indole scaffold with a pendant ethyl ester, enabling direct functionalization at the 3-position. This bench-stable derivative facilitates C–C and C–heteroatom coupling reactions in synthetic routes to bioactive indole alkaloids and pharmaceutical intermediates.
Ethyl 3-bromo-1H-indole-2-carboxylate serves as a versatile building block for the synthesis of substituted indoles and heterocyclic scaffolds. The bromo group at the 3-position enables efficient palladium-catalyzed cross-coupling reactions, while the ester functionality supports further transformations such as hydrolysis or reduction. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for medicinal chemistry applications and modular library synthesis.
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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: