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Structure of 56671-67-1
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Imidazo[1,5-a]pyridine-1-carbaldehyde features a rigid heterocyclic core with a strategically positioned aldehyde group. This configuration enables direct incorporation into diverse molecular architectures, particularly in medicinal chemistry and ligand design. The aldehyde moiety facilitates efficient derivatization via condensation reactions, offering rapid access to functionalized analogs under mild conditions.
Imidazo[1,5-a]pyridine-1-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. The aldehyde functionality facilitates reductive amination, Grignard additions, and Ugi-type reactions, while the fused imidazopyridine core exhibits good bench stability and compatibility with common protecting groups. Its defined regiochemistry supports predictable transformations in medicinal chemistry campaigns 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-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: