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Structure of 106012-56-0
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Imidazo[1,2-a]pyrimidine-3-carbaldehyde features a rigid heteroaromatic core with a strategically positioned aldehyde group, enabling direct functionalization in cross-coupling and condensation reactions. This scaffold integrates readily into bioactive molecule design, offering enhanced metabolic stability and predictable binding interactions in medicinal chemistry applications.
Imidazo[1,2-a]pyrimidine-3-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. The aldehyde functionality facilitates diverse transformations including reductive amination, Wittig reactions, and coupling with nucleophiles, while the fused imidazopyrimidine core exhibits good bench stability and compatibility with common protecting groups. Its well-defined reactivity profile supports integration into medicinal chemistry campaigns 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: