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Structure of 75806-86-9
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2-Bromo-5-chloro-3-nitropyridine features a triply substituted pyridine core with distinct halogen and nitro functionalities. The electron-deficient ring enables efficient coupling reactions, while the bromo and chloro groups provide orthogonal reactivity for sequential functionalization. This compound serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical candidates.
2-Bromo-5-chloro-3-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 compatibility with standard palladium-catalyzed transformations.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H318
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362-P501
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Lot numbers can be found on the outside label of a product: