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Structure of 73895-98-4
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6-Bromo-4-methylpyridin-2-amine features a bromine substituent at the 6-position and a methyl group at the 4-position on a pyridine core, enabling selective functionalization in cross-coupling reactions. The ortho-amino group facilitates metal coordination and conjugation, while the electron-deficient pyridine ring supports nucleophilic substitution. This scaffold delivers high reactivity under standard conditions and integrates efficiently into complex heterocyclic architectures.
6-Bromo-4-methylpyridin-2-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 enhances electron density at the pyridine ring, facilitating subsequent functionalization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for constructing heterocyclic scaffolds in 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: