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Structure of 1101120-37-9
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Pyrazolo[1,5-a]pyridin-5-amine delivers a rigid, electron-rich heterocyclic scaffold ideal for medicinal chemistry applications. This nitrogen-dense framework integrates readily into kinase inhibitors and other bioactive molecules, offering enhanced binding affinity through π-stacking and hydrogen-bonding interactions. The pendant amine enables direct derivatization, streamlining the synthesis of targeted compounds.
Pyrazolo[1,5-a]pyridin-5-amine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to kinase inhibitors and other bioactive scaffolds. Its electron-rich pyrazolo-pyridine core exhibits favorable reactivity in C–H functionalization and palladium-catalyzed couplings, while the primary amine facilitates downstream derivatization. The compound demonstrates good bench stability and compatibility with common protecting group strategies, supporting its use in multi-step synthesis and API development 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: