| 1. | Copper 8-hydroxyquinoline is sometimes included in paint to prevent mildew.
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| 2. | The compound is an 8-hydroxyquinoline, a common chelating agent.
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| 3. | There are also many non-antibacterial medical uses for 4-hydroxyquinoline.
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| 4. | Aniline reacts with another equivalent of benzoylacetanilide before forming the 4-hydroxyquinoline.
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| 5. | Continuation of this reaction using the Conrad-Limpach mechanism led to the synthesis of 2-hydroxyquinoline.
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| 6. | A 1964 study found that with certain reaction conditions formation of a 4-hydroxyquinoline is a competing reaction.
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| 7. | Furthermore, the type of solvent used is very important to ensuring high yields of the 4-hydroxyquinoline product.
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| 8. | The initial synthesis of 2-hydroxyquinoline from a ?-ketoanilide was reported in 1886 as the Knorr quinoline synthesis.
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| 9. | Thus, 8-hydroxyquinoline is potentially useful to control American plants that have become invasive weeds in the diffuse knapweed's native range.
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| 10. | SDB-005 is the indazole core analogue of PB-22 where the 8-hydroxyquinoline has also been replaced with a naphthalene group.
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