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Structure of 916326-37-9
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5-Bromo-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde features a brominated pyrazolopyridine core paired with an aldehyde handle, enabling direct conjugation in synthetic workflows. The electron-deficient heterocycle supports efficient transition-metal-catalyzed coupling, while the aldehyde group facilitates rapid derivatization under mild conditions. This scaffold integrates readily into bioactive molecule design and advanced materials synthesis.
5-Bromo-1H-pyrazolo[3,4-b]pyridine-3-carbaldehyde serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. The bromo and aldehyde functionalities enable sequential cross-coupling and functionalization reactions, facilitating access to diverse pyrazolopyridine derivatives. Its bench-stable nature and compatibility with palladium-catalyzed transformations support efficient synthesis in medicinal chemistry 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: