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Structure of 16234-14-3
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2,4-Dichlorothieno[3,2-d]pyrimidine features a fused thienopyrimidine core with strategically positioned chlorine atoms enhancing electrophilic reactivity. This electron-deficient heterocycle serves as a key scaffold in kinase inhibitor design and medicinal chemistry campaigns. The molecule exhibits robust stability under standard bench conditions and integrates readily into modular synthesis workflows.
2,4-Dichlorothieno[3,2-d]pyrimidine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of purine-like scaffolds. The dichloro substitution pattern facilitates regioselective cross-coupling and nucleophilic displacement reactions, while the thienopyrimidine core offers enhanced metabolic stability and favorable binding interactions. Bench-stable and amenable to purification via flash chromatography, it functions effectively in the synthesis of kinase inhibitors and other bioactive compounds.
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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: