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Structure of 56844-12-3
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6-Bromo-4-chlorothieno[2,3-d]pyrimidine features a fused thienopyrimidine core with complementary halogen substituents enabling selective cross-coupling. This electron-deficient heterocycle integrates readily into advanced pharmaceutical scaffolds, offering high functional group tolerance and stability under standard reaction conditions.
6-Bromo-4-chlorothieno[2,3-d]pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo and chloro substituents allow sequential functionalization, facilitating the construction of complex thienopyrimidine scaffolds relevant to medicinal chemistry. Its bench-stable crystalline form supports straightforward handling and purification, making it well-suited for iterative synthetic campaigns in API development.
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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: