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Structure of 116355-16-9
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Imidazo[1,2-a]pyridine-6-carbaldehyde features a fused heterocyclic core with a strategically positioned aldehyde group, enabling direct incorporation into bioactive molecule scaffolds. This electron-deficient platform facilitates efficient coupling reactions and serves as a key intermediate in the development of pharmaceutical candidates targeting kinase pathways.
Imidazo[1,2-a]pyridine-6-carbaldehyde serves as a versatile building block for heterocyclic synthesis, enabling efficient access to biologically relevant scaffolds. Its aldehyde functionality facilitates reductive amination, Wittig reactions, and condensation processes under standard conditions. The molecule exhibits good bench stability and functional group tolerance, making it suitable for iterative synthesis in 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 : H317
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Precautionary Statements : P261-P272-P280-P302+P352-P362+P364-P501
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Lot numbers can be found on the outside label of a product: