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Structure of 1260886-58-5
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6-Bromo-3-iodoquinolin-4-ol features a quinolin-4-ol scaffold bearing bromo and iodo substituents at the 6- and 3-positions, respectively. This electron-deficient heterocycle integrates readily into cross-coupling workflows, enabling efficient access to complex polycyclic architectures. The hydroxyl group enhances solubility and provides a handle for derivatization.
6-Bromo-3-iodoquinolin-4-ol serves as a versatile building block for the synthesis of functionalized quinoline scaffolds. The molecule features orthogonal halogen handles—bromine at C6 and iodine at C3—that enable sequential cross-coupling reactions under palladium catalysis. Its phenolic OH group provides a site for derivatization or metal coordination, enhancing utility in medicinal chemistry and materials science applications. Bench-stable and compatible with standard purification methods, it facilitates efficient access to complex heterocyclic architectures.
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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-P330-P362-P405-P501
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Lot numbers can be found on the outside label of a product: