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Structure of 66092-62-4
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2-Bromo-5-methyl-4-nitropyridine features a strategically positioned bromine atom and nitro group on a pyridine core, enabling direct functionalization in cross-coupling reactions. The methyl substituent enhances electron density at the 5-position, improving reactivity in palladium-catalyzed transformations. This bench-stable heterocycle integrates readily into complex molecular architectures.
2-Bromo-5-methyl-4-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined reactivity at the bromine site. The nitro group provides a handle for selective reduction or further functionalization, while the methyl substituent enhances electronic modulation and steric control. This compound exhibits excellent bench stability and facilitates efficient purification, making it ideal for constructing complex pyridine-based scaffolds 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: