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Structure of 84174-71-0
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7-Bromoquinolin-6-ol features a brominated quinoline scaffold with a phenolic hydroxyl group, enabling direct functionalization in cross-coupling and derivatization workflows. The electron-deficient aromatic system enhances reactivity in palladium-catalyzed transformations, while the hydroxyl moiety offers anchoring points for further conjugation. This bench-stable compound serves as a key intermediate in medicinal chemistry and materials synthesis.
7-Bromoquinolin-6-ol serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization at the C6 hydroxyl and C7 bromine sites. Its dual reactivity facilitates Suzuki-Miyaura coupling, nucleophilic substitution, and transition-metal-catalyzed cross-coupling reactions. The compound exhibits good bench stability and is readily purified by crystallization or flash chromatography, making it well-suited for scalable synthesis of quinoline-based pharmaceutical intermediates and heterocyclic scaffolds.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: