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Structure of 877-03-2
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5-Bromoindole-3-carboxaldehyde features a brominated indole core with a formyl group at the 3-position, enabling direct incorporation into heterocyclic scaffolds. This electron-deficient aldehyde facilitates efficient coupling reactions and serves as a key building block in medicinal chemistry and materials synthesis.
5-Bromoindole-3-carboxaldehyde serves as a versatile building block for the synthesis of functionalized indole scaffolds, enabling direct incorporation into biologically relevant heterocycles. Its aldehyde functionality facilitates efficient imine formation, reductive amination, and coupling reactions with nucleophiles under mild conditions. The bromo substituent provides a handle for subsequent palladium-catalyzed cross-coupling transformations, supporting modular diversification in medicinal chemistry and materials science applications. Bench-stable and readily purified by flash chromatography, it functions effectively in standard synthetic workflows.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: