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Structure of 596794-91-1
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Ethyl 4-chlorothieno[2,3-d]pyrimidine-6-carboxylate features a chlorinated thienopyrimidine core that enables direct functionalization in medicinal chemistry. This electron-deficient heterocycle integrates readily into kinase inhibitor scaffolds and serves as a key intermediate for bioactive purine analogs under standard conditions.
Ethyl 4-chlorothieno[2,3-d]pyrimidine-6-carboxylate serves as a versatile building block for the synthesis of thienopyrimidine-based heterocycles. The chloro group at the 4-position enables palladium-catalyzed cross-coupling reactions, while the ester functionality supports subsequent transformations into carboxylic acids or amides. Its bench-stable nature and compatibility with standard synthetic protocols make it well-suited for medicinal chemistry campaigns targeting kinase inhibitors and other bioactive scaffolds.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: