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Structure of 13877-56-0
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1H-Pyrazolo[4,3-d]pyrimidin-7-amine features a fused heterocyclic core with a primary amine at the C7 position, enabling direct functionalization in medicinal chemistry. This electron-rich scaffold integrates readily into kinase inhibitor designs and other bioactive architectures, offering enhanced binding affinity through hydrogen bonding and π-stacking interactions.
1H-Pyrazolo[4,3-d]pyrimidin-7-amine serves as a versatile heterocyclic building block for medicinal chemistry and catalytic synthesis. Its fused bicyclic core exhibits enhanced stability and predictable reactivity, enabling efficient functionalization at the 7-amino position. The scaffold functions effectively in transition-metal-catalyzed couplings and serves as a key intermediate in the construction of kinase inhibitors and other bioactive molecules.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3259
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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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: