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Structure of 14080-56-9
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Thieno[2,3-d]pyrimidin-4-amine features a fused heterocyclic core combining thiophene and pyrimidine moieties, delivering enhanced electron delocalization and planarity. This structural rigidity supports strong π-stacking interactions, making it ideal for applications in organic semiconductors and kinase inhibitor scaffolds. The amine functionality enables straightforward derivatization under mild conditions.
Thieno[2,3-d]pyrimidin-4-amine serves as a privileged heterocyclic scaffold in medicinal chemistry, enabling rapid access to bioactive compounds through its inherent planarity and hydrogen-bonding capacity. The molecule functions as a versatile building block for kinase inhibitors and other targeted therapeutics, exhibiting robust bench stability and compatibility with standard coupling reactions. Its functional group tolerance facilitates efficient derivatization at the amine and thienyl positions, supporting diverse analog generation in lead optimization campaigns.
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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: