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Structure of 1092351-49-9
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3-Bromo-1-methyl-1H-indazol-5-amine features a brominated indazole core with a methylated nitrogen and a primary amine at the 5-position, enabling direct functionalization in cross-coupling reactions. This electron-deficient scaffold serves as a key building block for bioactive molecules in medicinal chemistry, particularly in kinase inhibitor development. The bromine acts as a reactive handle for Pd-catalyzed transformations under standard conditions.
3-Bromo-1-methyl-1H-indazol-5-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its bromine substituent. The indazolyl scaffold provides structural rigidity and favorable pharmacophoric properties, while the methyl and amino groups offer sites for further functionalization. Its bench-stable nature and compatibility with standard reaction conditions facilitate efficient synthesis of complex heterocyclic architectures.
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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: