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Structure of 57473-32-2
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5,7-Dichloroimidazo[1,2-a]pyrimidine serves as a potent electrophilic scaffold in medicinal chemistry, featuring two chlorine substituents that enhance reactivity at the imidazopyrimidine core. This electron-deficient heterocycle integrates readily into kinase inhibitors and nucleoside analogs, offering high functional group tolerance and stability under standard bench conditions.
5,7-Dichloroimidazo[1,2-a]pyrimidine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to imidazo[1,2-a]pyrimidine scaffolds prevalent in medicinal chemistry. The dichloro substitution pattern provides orthogonal reactivity for nucleophilic displacement, facilitating the installation of diverse N- and C-substituents under mild conditions. Its bench-stable solid form and compatibility with standard coupling protocols make it ideal for high-throughput library generation and scale-up applications.
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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: