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Structure of 156118-16-0
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3-Amino-6-bromo-4-methylpyridine features a pyridine core functionalized with amino, bromo, and methyl groups at strategic positions, enabling selective coupling reactions. The electron-donating amino group enhances reactivity in cross-coupling processes, while the bromo handle facilitates palladium-catalyzed transformations. This scaffold offers tunable electronic properties for pharmaceutical intermediates and advanced materials synthesis under standard conditions.
3-Amino-6-bromo-4-methylpyridine serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The amino and bromo groups offer orthogonal reactivity for sequential derivatization, while the methyl group enhances metabolic stability. Bench-stable and readily purified by recrystallization, it functions effectively in standard coupling protocols and heterocyclic scaffold elaboration.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: