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Structure of 138891-58-4
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Ethyl 3-bromoimidazo[1,5-a]pyridine-1-carboxylate features a brominated imidazopyridine core with enhanced reactivity at the 3-position, enabling direct functionalization in cross-coupling processes. The ester group provides solubility and stability under standard conditions, facilitating integration into synthetic sequences for pharmaceutical intermediates and advanced heterocyclic architectures.
Ethyl 3-bromoimidazo[1,5-a]pyridine-1-carboxylate serves as a versatile building block for the synthesis of imidazo[1,5-a]pyridine derivatives, key scaffolds in medicinal chemistry. The bromine at the 3-position enables facile palladium-catalyzed cross-coupling reactions, while the ester group supports further functionalization. Its bench-stable nature and compatibility with diverse reaction conditions facilitate efficient access to complex heterocyclic architectures relevant to drug discovery and process development.
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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: