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Structure of 1137475-57-0
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2-Bromo-4-chloro-5-nitropyridine features a tri-functional pyridine core with distinct halogen and nitro substituents, enabling selective cross-coupling and functionalization. The electron-deficient ring facilitates palladium-catalyzed reactions, while the bromo and chloro groups offer orthogonal reactivity for sequential transformations. This compound serves as a key intermediate in medicinal chemistry and agrochemical synthesis, where precise molecular editing is essential.
2-Bromo-4-chloro-5-nitropyridine serves as a versatile building block for the synthesis of functionalized pyridine derivatives. Its orthogonal halogenation pattern enables sequential cross-coupling reactions, facilitating the construction of complex heterocyclic scaffolds. The nitro group provides a handle for reduction and subsequent derivatization, while the molecule exhibits good bench stability and ease of purification, making it suitable for iterative synthetic workflows in medicinal chemistry and process 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: