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Structure of 83255-86-1
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3-Bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine features a brominated pyrazolopyrimidine core with a primary amine at the 4-position, enabling direct coupling in cross-coupling reactions. The electron-deficient heterocycle facilitates efficient functionalization, while the bromide serves as a reactive handle for palladium-catalyzed transformations. This scaffold exhibits excellent stability under standard conditions and integrates readily into medicinal chemistry campaigns targeting kinase inhibitors and nucleoside analogs.
3-Bromo-1H-pyrazolo[3,4-d]pyrimidin-4-amine serves as a versatile building block for purine-derived heterocycles, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling. The bromo group facilitates Suzuki, Stille, and Buchwald-Hartwig reactions, while the pyrazolo[3,4-d]pyrimidine core provides a stable scaffold with enhanced solubility and metabolic resistance. Bench-stable and readily purified by flash chromatography, it functions as a key intermediate in the synthesis of kinase inhibitors and nucleoside analogs.
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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: