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Structure of 1186608-71-8
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3-Bromo-1H-pyrazolo[3,4-b]pyridin-5-amine features a brominated pyrazolopyridine core with a primary amine at the 5-position, enabling direct coupling in cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-catalyzed transformations, while the amine group serves as a handle for further functionalization. This scaffold demonstrates stability under standard reaction conditions and is well-suited for medicinal chemistry campaigns targeting kinase inhibitors and other bioactive molecules.
3-Bromo-1H-pyrazolo[3,4-b]pyridin-5-amine serves as a versatile building block for the synthesis of bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions due to its stable bromo functionality and electron-deficient pyrazolopyridine core. Its amine group provides a handle for derivatization, while the molecule exhibits good bench stability and compatibility with standard purification techniques, facilitating integration into medicinal chemistry and process development 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: