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Structure of 1211516-09-4
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6-Bromo-1H-pyrazolo[4,3-b]pyridin-3-amine features a brominated pyrazolopyridine core with a primary amine at the 3-position, enabling direct coupling in cross-coupling reactions. The electron-deficient heterocycle facilitates metal-catalyzed transformations, while the amine group serves as a handle for derivatization. This scaffold offers enhanced stability and solubility in polar solvents, supporting efficient synthesis of bioactive compounds.
6-Bromo-1H-pyrazolo[4,3-b]pyridin-3-amine serves as a versatile building block for the synthesis of biologically relevant heterocycles. The bromine and amino groups enable efficient late-stage functionalization via palladium-catalyzed cross-coupling and electrophilic substitution reactions. Its bench-stable nature and compatibility with diverse reaction conditions facilitate rapid access to pyrazolopyridine-based scaffolds used in medicinal chemistry and agrochemical research.
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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: