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Structure of 934560-92-6
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6-Bromo-1H-pyrazolo[3,4-b]pyridine features a fused heterocyclic core with a bromine substituent at the 6-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into pharmaceutical and agrochemical scaffolds, offering high reactivity under standard palladium-catalyzed conditions. The molecule exhibits bench-stable handling and compatibility with diverse synthetic transformations.
6-Bromo-1H-pyrazolo[3,4-b]pyridine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. Its bromo substituent facilitates efficient C–C and C–heteroatom bond formation, making it well-suited for constructing complex scaffolds in medicinal chemistry and materials science. The compound exhibits excellent bench stability and ease of purification, supporting reliable integration into multi-step synthetic sequences.
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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: