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Structure of 10460-50-1
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4-Amino-5-bromo-2-methylpyridine features a pyridine core functionalized with amino, bromo, and methyl groups at distinct positions, enabling selective coupling reactions. The electron-donating amino group enhances reactivity in cross-coupling processes, while the bromo substituent serves as a reliable handle for palladium-catalyzed transformations. This molecule combines synthetic versatility with bench-stable handling, making it well-suited for building complex heterocyclic architectures in medicinal chemistry and materials science applications.
4-Amino-5-bromo-2-methylpyridine serves as a versatile building block for the synthesis of bioactive heterocycles and pharmaceutical intermediates. The amino group enables direct coupling reactions, while the bromo substituent facilitates palladium-catalyzed cross-couplings. The methyl group enhances metabolic stability and modulates electronic properties. This compound exhibits excellent bench stability and is compatible with standard purification protocols, making it ideal for iterative synthetic workflows in medicinal chemistry and process 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: