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Structure of 1511297-53-2
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2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine features a fused heterocyclic core with a chlorine atom at the 2-position and a methyl group at the 5-position, providing a robust scaffold for nucleophilic substitution reactions. This electron-deficient pyrrolopyrimidine integrates readily into pharmaceutical intermediates and functional materials, offering high reactivity under standard conditions while maintaining bench stability.
2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-derived scaffolds. Its chloro group at the C2 position facilitates nucleophilic substitution reactions, while the methyl substituent enhances metabolic stability and modulates electronic properties. The compound 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 : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P405-P501
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Lot numbers can be found on the outside label of a product: