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Structure of 63572-73-6
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5-Nitro-1H-pyrazolo[3,4-b]pyridine features a fused heterocyclic core with a nitro group at the 5-position, imparting electron-deficient character ideal for cross-coupling reactions. This bench-stable scaffold integrates readily into bioactive molecule design, offering enhanced solubility and reactivity in medicinal chemistry applications.
5-Nitro-1H-pyrazolo[3,4-b]pyridine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its electron-deficient pyrazolopyridine core facilitates electrophilic substitution and transition-metal-catalyzed coupling reactions. The nitro group enables further functionalization via reduction or nucleophilic displacement, offering access to diverse scaffolds. Bench-stable and compatible with common purification methods, it functions reliably in multi-step syntheses.
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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: