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Structure of 1618-36-6
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4-Chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a critical heterocyclic scaffold in medicinal chemistry, offering a rigid, electron-deficient core for targeted kinase inhibition. This bench-stable building block integrates readily into purine analogs and bioactive molecules, enabling efficient access to advanced intermediates in drug discovery pipelines.
4-Chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient access to purine-derived scaffolds. Its well-defined reactivity at the C4 position facilitates palladium-catalyzed cross-coupling reactions, while the methyl group provides a handle for further functionalization. The compound exhibits excellent bench stability and compatibility with standard synthetic workflows, making it a practical choice for the construction of kinase inhibitors and other biologically active heterocycles.
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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: