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Structure of 1119280-68-0
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2-Chlorothieno[3,2-d]pyrimidine features a fused thienopyrimidine core with a chlorine substituent at the 2-position, delivering enhanced electron deficiency and improved metabolic stability. This scaffold integrates readily into kinase inhibitors and bioactive heterocycles, offering high reactivity in cross-coupling and nucleophilic substitution reactions under standard conditions.
2-Chlorothieno[3,2-d]pyrimidine serves as a versatile heterocyclic building block for medicinal chemistry and materials science, enabling efficient construction of kinase inhibitors and functionalized π-conjugated systems. Its chlorine substituent facilitates palladium-catalyzed cross-coupling reactions, while the fused thienopyrimidine core provides enhanced metabolic stability and planar rigidity. The compound exhibits excellent bench stability and compatibility with diverse reaction conditions, making it a practical scaffold for high-throughput synthesis and API development.
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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: