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Structure of 100367-40-6
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2-Amino-5-bromo-4-methyl-3-nitropyridine features a fused pyridine core bearing strategically positioned amino, bromo, methyl, and nitro substituents. This electron-deficient heterocycle enables direct functionalization in cross-coupling and cyclization reactions. The ortho-nitro group enhances reactivity toward nucleophilic substitution, while the amino handle supports derivatization. Bench-stable under standard conditions, it serves as a key intermediate for bioactive molecule synthesis.
2-Amino-5-bromo-4-methyl-3-nitropyridine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via cross-coupling and reduction strategies. Its complementary functional groups—bromine for Pd-catalyzed coupling, nitro for selective reduction, and amino/methyl groups for derivatization—offer high synthetic flexibility. Bench-stable and compatible with standard purification methods, it facilitates rapid prototyping in medicinal chemistry and materials science applications.
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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: