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Structure of 2139336-89-1
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This pyrrolopyrimidine scaffold features two chlorine substituents at the 2,4-positions, enhancing electron deficiency and enabling selective coupling in cross-coupling reactions. The dihydro structure provides a stable, bench-ready platform for synthesizing kinase inhibitors and nucleoside analogs.
2,4-Dichloro-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block for purine-based heterocycles, enabling efficient construction of biologically relevant scaffolds. Its dichloro substitution pattern facilitates selective nucleophilic displacement reactions, offering high functional group tolerance and bench stability. The compound functions effectively in Pd-catalyzed cross-coupling and amine displacement protocols, supporting scalable synthesis of kinase inhibitors and other medicinal chemistry targets.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: