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Structure of 68618-36-0
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3-Bromo-1H-pyrazolo[3,4-b]pyridine features a fused heterocyclic core with a bromine substituent at the 3-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold integrates readily into pharmaceutical and agrochemical discovery pipelines, offering high reactivity under standard palladium-catalyzed conditions.
3-Bromo-1H-pyrazolo[3,4-b]pyridine serves as a versatile building block for heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions with high efficiency. The bromo group facilitates reliable functionalization in Suzuki, Stille, and Negishi transformations, while the fused pyrazolo-pyridine core provides inherent stability and favorable electronic properties for medicinal chemistry applications. This compound exhibits excellent bench stability and simplifies purification, making it well-suited for iterative synthesis of complex nitrogen-containing scaffolds.
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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 : 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: