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Structure of 871254-63-6
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6-Chloro-3-methyl-1H-pyrazolo[3,4-d]pyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering a rigid, electron-deficient core for targeted molecular design. This bench-stable compound integrates readily into kinase inhibitor frameworks and other bioactive architectures, enabling efficient access to functionalized purine analogs under standard conditions.
6-Chloro-3-methyl-1H-pyrazolo[3,4-d]pyrimidine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient construction of pyrazolo[3,4-d]pyrimidine scaffolds. The chloro group facilitates nucleophilic substitution reactions, while the methyl substituent enhances stability and modulates reactivity. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for medicinal chemistry campaigns and process-scale applications.
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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: