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Structure of 97944-46-2
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2-Bromo-6-methyl-4-nitropyridine is a halogenated pyridine derivative featuring a nitro group at C4 and a methyl substituent at C6. This electron-deficient heterocycle serves as a key intermediate in the synthesis of bioactive molecules, enabling efficient coupling reactions through its reactive bromine site. The compound exhibits good stability under standard bench conditions and facilitates modular construction in medicinal chemistry workflows.
2-Bromo-6-methyl-4-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromide and electron-deficient pyridine core. The methyl and nitro groups provide orthogonal functional handles for further derivatization. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis of complex nitrogen-containing 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: