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Structure of 788819-82-9
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Imidazo[1,2-a]pyrazine-6-carboxylic acid features a fused heterocyclic core with a carboxylic acid at the C6 position, enabling direct conjugation in medicinal chemistry. The electron-deficient scaffold supports hydrogen bonding and dipole interactions, enhancing target binding in kinase inhibitors and bioactive molecule design. This bench-stable derivative integrates readily into synthetic sequences under standard conditions.
Imidazo[1,2-a]pyrazine-6-carboxylic acid serves as a versatile heterocyclic building block in medicinal chemistry, enabling the construction of bioactive scaffolds through standard amide coupling and derivatization protocols. Its carboxylic acid functionality facilitates conjugation with amines, while the fused imidazo[1,2-a]pyrazine core provides structural rigidity and favorable pharmacophoric properties for target engagement. The compound exhibits good bench stability and compatibility with common purification methods, making it well-suited for iterative synthesis campaigns in drug discovery.
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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: