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Structure of 953411-10-4
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7-Bromo-1H-indazol-5-amine features a brominated indazole scaffold with a primary amine at the 5-position, enabling direct coupling in C–N cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in transition-metal-catalyzed transformations, while the bench-stable, moisture-tolerant structure supports reliable handling in synthetic workflows.
7-Bromo-1H-indazol-5-amine serves as a versatile building block in medicinal chemistry, enabling direct incorporation into biologically active scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates efficient functionalization, while the primary amine supports derivatization through acylation, alkylation, or reductive amination. Its stability under standard reaction conditions and compatibility with diverse coupling partners make it a practical choice for constructing heterocyclic libraries and lead optimization campaigns.
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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: