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Structure of 79055-61-1
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2-Bromo-3-methylpyridin-4-amine features a bromine substituent at the 2-position and a methyl group at the 3-position on a pyridine core bearing a primary amine at the 4-position. This electron-deficient heterocycle serves as a key intermediate in medicinal chemistry, enabling direct functionalization via palladium-catalyzed cross-coupling. The molecule exhibits bench-stable handling and compatibility with standard reaction conditions.
2-Bromo-3-methylpyridin-4-amine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine and amine functionalities. The methyl group provides steric and electronic modulation, while the pyridine core offers compatibility with standard heterocyclic synthesis protocols. Bench-stable and readily purified, it facilitates efficient construction of complex nitrogen-containing scaffolds relevant to API development.
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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: