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Structure of 100644-65-3
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4-Chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine serves as a critical heterocyclic scaffold in medicinal chemistry, featuring a chlorine atom at the 4-position and an amine group at C6. This configuration enables direct incorporation into kinase inhibitors and antiviral agents, where its electron-deficient core enhances target binding affinity. The compound exhibits bench-stable handling characteristics and compatibility with standard coupling reactions.
4-Chloro-1H-pyrazolo[3,4-d]pyrimidin-6-amine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling efficient access to pyrazolopyrimidine scaffolds prevalent in kinase inhibitors and antiviral agents. The chloro group facilitates nucleophilic substitution reactions, while the amine functionality supports derivatization via coupling protocols. Bench-stable and readily purified by recrystallization, it functions reliably in standard medicinal chemistry workflows.
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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: