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Structure of 90213-66-4
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2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine is a heterocyclic scaffold featuring two chlorine substituents at electron-deficient positions, enabling efficient coupling in transition-metal-catalyzed reactions. This bench-stable core integrates readily into pharmaceutical and agrochemical architectures, offering enhanced reactivity and selectivity in C–H functionalization processes.
2,4-Dichloro-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-based heterocycles. Its dichloro substitution pattern facilitates selective palladium-catalyzed cross-coupling reactions and nucleophilic aromatic substitution, supporting the synthesis of biologically active scaffolds. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthetic campaigns in drug discovery.
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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: