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Structure of 6752-16-5
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3-Aminopyrazolo[3,4-b]pyridine delivers a nitrogen-rich heterocyclic scaffold with enhanced electron density at the pyrazole ring, enabling direct integration into bioactive molecule design. This bench-stable, moisture-tolerant core pairs effectively in transition-metal-catalyzed coupling reactions and serves as a strategic anchor for kinase inhibitors and fluorescent probes.
3-Aminopyrazolo[3,4-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and catalyst development. Its fused tricyclic structure enables direct functionalization at the amine and pyridine positions, supporting diverse coupling reactions and derivatization workflows. The compound exhibits good bench stability and facilitates efficient incorporation into bioactive scaffolds due to its favorable solubility and compatibility with standard synthetic protocols.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301
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Precautionary Statements : P264-P270-P330-P405-P501
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Lot numbers can be found on the outside label of a product: