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Structure of 1049706-73-1
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3-Bromo-2-chloro-4-methyl-5-nitropyridine features a densely functionalized pyridine core with complementary electrophilic sites for cross-coupling and nucleophilic substitution. The nitro group enhances reactivity at C5, while the methyl substituent provides steric and electronic modulation. This compound serves as a versatile intermediate in medicinal chemistry and agrochemical synthesis.
3-Bromo-2-chloro-4-methyl-5-nitropyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates selective functionalization under standard Suzuki or Stille conditions, while the chloro and nitro substituents provide complementary reactivity and electronic modulation. Bench-stable and compatible with common protecting group strategies, it functions effectively in the construction of substituted pyridine scaffolds relevant to medicinal chemistry and agrochemical research.
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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: