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Structure of 1203181-56-9
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3-Bromo-1-methyl-1H-indazol-6-amine features a brominated indazoline core with a methylated nitrogen and a primary amine at the 6-position, enabling direct coupling in Suzuki-Miyaura and Buchwald-Hartwig reactions. This bench-stable scaffold integrates readily into bioactive heterocycles for medicinal chemistry applications.
3-Bromo-1-methyl-1H-indazol-6-amine serves as a versatile building block for constructing biologically active heterocycles, enabling palladium-catalyzed cross-coupling reactions with broad functional group tolerance. The bromo group facilitates efficient C–C and C–N bond formation, while the indazol-6-amine scaffold provides a rigid, polar platform suitable for medicinal chemistry optimization. Bench-stable and readily purified, it functions effectively in standard coupling protocols and supports scalable synthesis of kinase inhibitors and other pharmaceutical intermediates.
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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: