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Structure of 30384-96-4
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6-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde features a brominated imidazopyridine core paired with a reactive aldehyde group, enabling direct functionalization in cross-coupling and conjugation workflows. The electron-deficient heterocycle enhances compatibility with nucleophilic attack, while the aldehyde facilitates rapid derivatization under mild conditions. This scaffold delivers high stability and predictable reactivity in synthetic medicinal chemistry and materials development.
6-Bromoimidazo[1,2-a]pyridine-3-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of pharmacologically relevant scaffolds. Its bromo and aldehyde functionalities provide orthogonal handles for Pd-catalyzed cross-coupling and condensation reactions, facilitating rapid diversification in medicinal chemistry campaigns. The compound exhibits good bench stability and is amenable to standard purification techniques, making it well-suited for high-throughput 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 : 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: