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Structure of 16269-66-2
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4-Chlorothieno[3,2-d]pyrimidine serves as a critical heterocyclic scaffold in medicinal chemistry, featuring a fused thienopyrimidine core with a chlorine substituent at the 4-position. This electron-deficient system enables direct incorporation into kinase inhibitors and other bioactive molecules through cross-coupling reactions. The compound exhibits high stability under standard conditions and facilitates efficient derivatization for targeted drug discovery applications.
4-Chlorothieno[3,2-d]pyrimidine serves as a versatile building block for the synthesis of heterocyclic compounds, particularly in medicinal chemistry and agrochemical research. Its chloro substituent enables facile palladium-catalyzed cross-coupling reactions, while the fused thienopyrimidine core provides structural rigidity and enhanced electronic properties. The compound exhibits good bench stability and compatibility with common functional groups, facilitating efficient derivatization in multi-step synthetic sequences.
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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: