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Structure of 1186115-39-8
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4-Bromo-5-iodopyridin-2-amine features a dual halogenated pyridine core with bromo and iodo substituents at adjacent positions, enabling efficient cross-coupling transformations. The amino group at C2 provides a reactive handle for nucleophilic functionalization, while the electron-deficient aromatic system enhances compatibility with palladium-catalyzed reactions. This compound serves as a key building block in the synthesis of advanced pharmaceutical intermediates and functionalized heterocycles.
4-Bromo-5-iodopyridin-2-amine serves as a versatile building block in cross-coupling chemistry, enabling the construction of biaryl and heterocyclic scaffolds. The bromo and iodo substituents provide orthogonal reactivity for Pd-catalyzed coupling reactions, while the pyridin-2-amine functionality offers a handle for further derivatization. Its bench-stable nature and compatibility with standard reaction conditions make it well-suited for medicinal chemistry and process development workflows.
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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: