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Structure of 1192711-71-9
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This pyrrolo[2,3-d]pyrimidine scaffold features a methyl group at C6 and chlorine atoms at C2 and C4, delivering enhanced electron-withdrawing character and improved metabolic stability. The fused heterocyclic system enables direct incorporation into kinase inhibitors and nucleoside analogs, serving as a key building block in medicinal chemistry campaigns targeting purine-binding sites.
2,4-Dichloro-6-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block for purine-based scaffolds in medicinal chemistry. The dichloro substitution enables regioselective palladium-catalyzed cross-coupling reactions, while the methyl group enhances metabolic stability. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for modular synthesis of kinase inhibitors and antiviral agents.
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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: