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Structure of 814918-95-1
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5-Bromo-4-chlorothieno[2,3-d]pyrimidine features a fused thienopyrimidine core with complementary halogenation at the 5-bromo and 4-chloro positions, enabling selective cross-coupling reactions. This electron-deficient heterocycle integrates readily into pharmaceutical scaffolds and serves as a key intermediate in medicinal chemistry.
5-Bromo-4-chlorothieno[2,3-d]pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of advanced pharmaceutical scaffolds. Its complementary halogenation pattern facilitates palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The molecule exhibits excellent bench stability and simplifies purification due to its crystalline nature, making it well-suited for iterative synthetic sequences in medicinal chemistry and process 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: