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Structure of 1060816-67-2
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2-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine delivers a reactive chloro handle at C2 and a methyl group at C7, enabling efficient coupling in heterocyclic synthesis. This bench-stable scaffold integrates readily into purine analogs and kinase inhibitor frameworks, offering enhanced solubility and regioselective functionalization under standard conditions.
2-Chloro-7-methyl-7H-pyrrolo[2,3-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-like scaffolds. Its chloro group at the C2 position facilitates nucleophilic substitution reactions, while the methyl substituent at C7 enhances metabolic stability and modulates electronic properties. The scaffold exhibits excellent bench stability and compatibility with standard coupling protocols, making it ideal for the synthesis of kinase inhibitors and other bioactive 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: