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Structure of 89856-44-0
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5-Bromo-4,6-dimethylpyridin-2-amine features a pyridine core functionalized with bromo and methyl groups at strategic positions, enabling selective coupling in cross-coupling reactions. The electron-deficient nitrogen atom enhances reactivity in palladium-catalyzed transformations. This bench-stable derivative integrates readily into complex molecular architectures under standard conditions.
5-Bromo-4,6-dimethylpyridin-2-amine serves as a versatile building block in medicinal chemistry and catalytic synthesis. The bromine substituent enables palladium-catalyzed cross-coupling reactions, while the pyridin-2-amine functionality provides a robust site for metal coordination and further derivatization. Its methyl groups enhance stability and modulate electronic properties, contributing to favorable solubility and handling characteristics. This compound facilitates efficient access to substituted heterocycles and functionalized scaffolds common in API development.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H317-H318
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Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: