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Structure of 56844-38-3
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2,4-Dichloro-5-methylthieno[2,3-d]pyrimidine features a fused thienopyrimidine core with strategically positioned chloro and methyl substituents, delivering enhanced reactivity in cross-coupling transformations. This electron-deficient scaffold integrates readily into advanced heterocyclic architectures, enabling efficient access to functionalized pyrimidine derivatives under standard conditions.
2,4-Dichloro-5-methylthieno[2,3-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine and pyrimidine-based heterocycles. Its dichloro substitution pattern facilitates nucleophilic displacement reactions, while the methylthienopyrimidine core provides structural rigidity and favorable electronic properties. The compound exhibits excellent bench stability and compatibility with standard coupling protocols, supporting scalable synthesis of 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 : 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: