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Structure of 1194375-12-6
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8-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde features a brominated imidazopyridine core paired with a reactive aldehyde handle, enabling direct conjugation in medicinal chemistry. This bench-stable scaffold integrates readily into bioactive molecules, offering enhanced electronic and steric profiles for targeted ligand design.
8-Bromoimidazo[1,2-a]pyridine-2-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of imidazo[1,2-a]pyridine-based scaffolds. The aldehyde functionality facilitates nucleophilic additions and condensation reactions, while the bromo substituent supports palladium-catalyzed cross-coupling transformations. Its bench-stable nature and compatibility with diverse functional groups make it well-suited for medicinal chemistry and process development 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: