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Structure of 947534-69-2
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2,5-Dibromo-4-methyl-3-nitropyridine features a sterically hindered pyridine core bearing two bromine atoms at positions 2 and 5, a methyl group at C4, and a nitro group at C3. This electron-deficient heterocycle serves as a key building block for constructing complex nitrogen-containing scaffolds in medicinal chemistry and materials science. The molecule exhibits enhanced stability under standard handling conditions and integrates readily into cross-coupling reactions.
2,5-Dibromo-4-methyl-3-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the 2- and 5-positions via palladium-catalyzed cross-coupling reactions. The nitro group facilitates subsequent reduction and substitution, while the methyl substituent provides steric and electronic modulation. Its bench-stable crystalline form and predictable reactivity profile support efficient synthesis of complex pyridine-based scaffolds relevant to agrochemical and pharmaceutical 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-H320-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: