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Structure of 23056-47-5
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2-Bromo-4-methyl-5-nitropyridine features a nitro group at the pyridine ring’s C5 position, enhancing electrophilicity for cross-coupling reactions. The bromine at C2 enables palladium-catalyzed transformations, while the methyl substituent provides steric and electronic modulation. This compound serves as a key intermediate in pharmaceutical synthesis and functional materials development under standard conditions.
2-Bromo-4-methyl-5-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined electrophilic sites. The bromo group facilitates Suzuki, Stille, and Negishi couplings, while the nitro and methyl functionalities offer orthogonal reactivity for downstream functionalization. Its bench-stable crystalline form supports reliable handling and purification, making it suitable for iterative synthesis of complex pyridine-based scaffolds.
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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: