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Structure of 31169-27-4
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7-Bromo-4-chlorothieno[3,2-d]pyrimidine features a fused heterocyclic core with complementary halogen substituents at the 7- and 4-positions. This electron-deficient scaffold enables direct functionalization in cross-coupling reactions, serving as a key building block for advanced pharmaceutical intermediates and agrochemicals.
7-Bromo-4-chlorothieno[3,2-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling the construction of biologically active heterocyclic scaffolds. Its well-defined reactivity profile facilitates palladium-catalyzed cross-coupling reactions and nucleophilic substitution processes, with both halogens offering orthogonal functionalization potential. The molecule exhibits excellent bench stability and compatibility with standard synthetic workflows, making it ideal for the modular synthesis of advanced pharmaceutical intermediates and kinase inhibitors.
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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: