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Structure of 118000-43-4
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Imidazo[1,2-a]pyridine-2-carbaldehyde features a fused heterocyclic core with a reactive aldehyde group at the 2-position. This configuration enables direct incorporation into bioactive molecule scaffolds, particularly in kinase inhibitor and fluorescent probe development. The electron-deficient imidazopyridine ring enhances conjugation potential, while the aldehyde facilitates efficient coupling reactions under mild conditions.
Imidazo[1,2-a]pyridine-2-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds through standard condensation and coupling reactions. Its aldehyde functionality facilitates efficient derivatization via reductive amination, Wittig-type transformations, and nucleophilic addition, while maintaining bench stability and compatibility with common protecting group strategies.
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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: