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Structure of 23002-51-9
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6-Chloro-1H-pyrazolo[3,4-d]pyrimidine is a bench-stable heterocyclic scaffold featuring a chlorine substituent at the 6-position, enabling direct functionalization in late-stage synthesis. This electron-deficient core integrates readily into kinase inhibitor architectures and serves as a key building block for bioactive molecules in medicinal chemistry.
6-Chloro-1H-pyrazolo[3,4-d]pyrimidine serves as a versatile building block for heterocyclic synthesis, enabling efficient construction of pyrazolo[3,4-d]pyrimidine-based scaffolds. The chlorine atom at the C6 position facilitates nucleophilic substitution reactions with amines, thiols, and other soft nucleophiles, offering straightforward access to diverse derivatives. Its bench-stable nature and compatibility with standard coupling protocols make it ideal for medicinal chemistry campaigns and API development.
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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: