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Structure of 944906-56-3
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6-Chloroimidazo[1,2-a]pyrimidine serves as a reactive heterocyclic scaffold for constructing bioactive molecules. This electron-deficient imidazopyrimidine integrates readily into pharmaceutical intermediates and functional materials, offering high stability under standard conditions. The chloro substituent enables direct coupling reactions, streamlining synthetic access to complex architectures in medicinal chemistry and agrochemical development.
6-Chloroimidazo[1,2-a]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of imidazopyrimidine scaffolds prevalent in kinase inhibitors and antiviral agents. The chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the fused heterocyclic core exhibits excellent bench stability and compatibility with diverse functional groups. Its predictable reactivity supports straightforward incorporation into complex molecular architectures.
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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: