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Structure of 1180678-40-3
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5-Bromo-2-iodopyridin-3-amine delivers a dual halogenation pattern ideal for palladium-catalyzed cross-coupling reactions. The electron-deficient pyridine core supports efficient functionalization, while the bromo and iodo substituents enable sequential derivatization. This bifunctional scaffold facilitates rapid access to complex heterocyclic architectures in medicinal chemistry and materials science.
5-Bromo-2-iodopyridin-3-amine serves as a versatile building block for cross-coupling reactions, enabling the construction of biologically relevant heterocyclic scaffolds. The orthogonal reactivity of bromo and iodo groups facilitates sequential Pd-catalyzed couplings, while the pyridin-3-amine functionality provides a handle for further derivatization. Bench-stable and compatible with standard reaction conditions, it is well-suited for iterative synthesis in medicinal chemistry and materials science applications.
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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: