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Structure of 94220-43-6
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7-Chloro-1H-pyrazolo[4,3-b]pyridine is a heterocyclic scaffold featuring a chlorinated pyrazolopyridine core with enhanced electron-deficient character. This structural motif integrates readily into medicinal chemistry campaigns, serving as a key pharmacophore in kinase inhibitors and CNS-targeted therapeutics. The chlorine substituent enables site-specific derivatization through palladium-catalyzed cross-coupling reactions. Bench-stable and moisture-tolerant, it offers reliable performance in synthetic workflows across diverse reaction conditions.
7-Chloro-1H-pyrazolo[4,3-b]pyridine serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to bioactive scaffolds through palladium-catalyzed cross-coupling reactions. Its chloro substituent facilitates direct functionalization at the C7 position, while the fused pyrazolo[4,3-b]pyridine core exhibits favorable stability and compatibility with diverse reaction conditions. This compound functions as a key intermediate in the synthesis of kinase inhibitors and other pharmaceutical candidates, offering predictable reactivity and straightforward purification.
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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: