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Structure of 1368231-70-2
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4-Bromo-1H-indole-2-carboxaldehyde features a brominated indole core with a strategically positioned aldehyde group, enabling direct incorporation into diverse synthetic scaffolds. This bench-stable, moisture-tolerant reagent facilitates efficient access to biologically active heterocycles through C–H functionalization and condensation reactions under mild conditions.
4-Bromo-1H-indole-2-carboxaldehyde serves as a versatile building block in medicinal chemistry and synthetic organic chemistry, enabling efficient access to substituted indole scaffolds. The aldehyde functionality facilitates reductive amination, Grignard additions, and Ugi-type condensations, while the bromine substituent supports palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for modular synthesis of bioactive molecules and heterocyclic libraries.
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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: