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Structure of 1242140-62-0
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Ethyl 2-amino-5-bromo-1H-indole-3-carboxylate features a brominated indole core with a strategically positioned amino group and ester functionality, enabling direct incorporation into diverse heterocyclic scaffolds. The electron-rich indole system facilitates palladium-catalyzed coupling reactions, while the bench-stable nature simplifies handling in synthetic workflows.
Ethyl 2-amino-5-bromo-1H-indole-3-carboxylate serves as a versatile building block in the synthesis of indole-based pharmaceutical intermediates. The molecule combines a bromo substituent at C5 with an amino group at C2, enabling palladium-catalyzed cross-coupling reactions and directed functionalization. Its ethyl ester group facilitates subsequent transformations, including hydrolysis and amidation. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses targeting bioactive heterocycles.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: