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Structure of 90213-67-5
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2,4-Dichloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, featuring electron-deficient aromaticity and steric bulk at the 7-position. This configuration enhances reactivity in cross-coupling processes and supports incorporation into kinase inhibitors and nucleoside analogs. The molecule exhibits bench-stable handling characteristics and tolerates diverse reaction conditions.
2,4-Dichloro-7-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 cross-coupling reactions, while the methyl group enhances metabolic stability. This compound exhibits excellent bench stability and facilitates efficient functionalization under standard Pd-catalyzed conditions, making it well-suited for the synthesis of kinase inhibitors and nucleoside analogs.
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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: