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Structure of 143982-40-5
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Imidazo[1,2-a]pyrimidine-2-carbaldehyde features a rigid fused heterocyclic core paired with a reactive aldehyde group, enabling direct incorporation into bioactive scaffolds. This electron-deficient platform facilitates efficient coupling reactions and serves as a key intermediate in the synthesis of kinase inhibitors and antiviral agents.
Imidazo[1,2-a]pyrimidine-2-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its aldehyde functionality facilitates nucleophilic addition, reductive amination, and coupling reactions under mild conditions. The rigid, planar core exhibits excellent bench stability and functional group tolerance, making it well-suited for medicinal chemistry campaigns and process-scale applications in API 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: