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Structure of 478837-59-1
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3-Bromo-1H-indazol-5-amine features a brominated indazolyl scaffold with a strategically positioned amine at the 5-position, enabling direct functionalization in cross-coupling and bioconjugation workflows. The electron-rich aromatic core enhances reactivity in palladium-catalyzed transformations, while the bench-stable nature facilitates handling under standard conditions. This building block integrates seamlessly into medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds.
3-Bromo-1H-indazol-5-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions to access biologically active indazolyl scaffolds. The bromine and primary amine functionalities offer orthogonal reactivity for sequential derivatization, while the core heterocycle exhibits good bench stability and compatibility with standard purification methods.
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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: