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Structure of 137240-10-9
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4,5-Dichlorothieno[2,3-d]pyrimidine features a fused thienopyrimidine core with two chlorine substituents at the 4 and 5 positions, conferring enhanced electron-withdrawing character and improved metabolic stability. This scaffold serves as a critical building block in medicinal chemistry, particularly for kinase inhibitors and antiviral agents. The dichloro substitution pattern enables selective coupling reactions under standard conditions, facilitating rapid diversification in lead optimization campaigns.
4,5-Dichlorothieno[2,3-d]pyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to thienopyrimidine scaffolds prevalent in medicinal chemistry. The dichloro substitution pattern facilitates palladium-catalyzed cross-coupling reactions and nucleophilic aromatic substitution, offering predictable regioselectivity. Its bench-stable nature and compatibility with diverse functional groups make it a practical reagent for constructing complex molecular architectures in API development and target-oriented synthesis.
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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-H332-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: