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Structure of 126325-53-9
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2-Bromo-6-methylpyridin-3-amine features a bromine substituent at the 2-position and a methyl group at the 6-position, creating a sterically hindered, electron-deficient pyridine scaffold. This combination enables selective coupling reactions in late-stage functionalization, particularly in transition metal-catalyzed cross-couplings. The amine functionality provides a reactive handle for conjugation, facilitating integration into complex molecular architectures.
2-Bromo-6-methylpyridin-3-amine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine and amine functionalities. The methyl group enhances electronic modulation and metabolic stability in pharmaceutical scaffolds. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient access to complex pyridine-based architectures used in medicinal chemistry and agrochemical development.
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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: