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Structure of 577967-89-6
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2-Chloroquinolin-6-ol features a chlorinated quinoline scaffold with a phenolic hydroxyl group, enabling direct functionalization at the 6-position. This bench-stable, moisture-tolerant heterocycle serves as a key intermediate in pharmaceutical synthesis and ligand development, combining enhanced reactivity with structural rigidity for efficient coupling reactions under standard conditions.
2-Chloroquinolin-6-ol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C6 position via nucleophilic substitution or transition-metal-catalyzed coupling. Its stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient access to quinoline-based scaffolds common in kinase inhibitors and antimalarial agents.
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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: