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Structure of 1190927-74-2
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This bench-stable heterocyclic scaffold features a fused pyrrolopyrimidine core with strategically positioned chlorine atoms, enabling efficient coupling in C–H functionalization and transition-metal-catalyzed cross-coupling reactions. The hydrochloride salt enhances solubility and handling, facilitating use in synthetic medicinal chemistry workflows.
2,4-Dichloro-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidine hydrochloride serves as a versatile building block for purine-based heterocycles, enabling efficient access to nucleoside analogs and kinase inhibitor scaffolds. Its dichloro substitution pattern facilitates regioselective functionalization via palladium-catalyzed cross-coupling, while the hydrochloride salt enhances bench stability and simplifies purification. The compound functions effectively in standard amine displacement and cyclization protocols, offering reliable utility in medicinal chemistry campaigns targeting antiviral and anticancer 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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: