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Structure of 907945-69-1
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6-Bromoimidazo[1,2-a]pyrimidine-2-carboxylic acid features a fused heterocyclic core with a bromine substituent at the 6-position and a carboxylic acid group at C2, enabling direct functionalization in synthetic routes. This electron-deficient scaffold integrates readily into bioactive molecule frameworks, particularly in kinase inhibitor development and medicinal chemistry campaigns requiring halogenation handles for cross-coupling reactions.
6-Bromoimidazo[1,2-a]pyrimidine-2-carboxylic acid serves as a versatile building block for the synthesis of heterocyclic scaffolds in medicinal chemistry. Its bromine and carboxylic acid functionalities enable selective cross-coupling reactions and derivatization under standard conditions. The molecule exhibits good bench stability and facilitates efficient functional group manipulation, making it well-suited for constructing complex imidazopyrimidine-based frameworks used in drug discovery and materials science.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: