| Identification | Back Directory | [Name]
1-(8-hydroxyquinolin-5-yl)ethanone | [CAS]
2598-31-4 | [Synonyms]
NSC 40901
NSC 68447
NSC 523017
Quinacetol
5-Acetyloxine
5-Acetyl-8-quinolinol
1-(8-Hydroxyquinolin-5-yl)
5-Acetyl-8-hydroxyquinoline
1-(8-hydroxyquinolin-5-yl)ethanone
8-Hydroxy-5-quinolyl Methyl Ketone
Ethanone, 1-(8-hydroxy-5-quinolinyl)-
1-(8-hydroxyquinolin-5-yl)ethan-1-one | [Molecular Formula]
C11H9NO2 | [MDL Number]
MFCD00086061 | [MOL File]
2598-31-4.mol | [Molecular Weight]
187.19 |
| Chemical Properties | Back Directory | [Melting point ]
110-112°C | [Boiling point ]
321.94°C (rough estimate) | [density ]
1.1963 (rough estimate) | [refractive index ]
1.4900 (estimate) | [storage temp. ]
Refrigerator | [solubility ]
Chloroform, Methanol | [form ]
Solid | [pka]
3.70±0.10(Predicted) | [color ]
Pale Brown |
| Hazard Information | Back Directory | [Chemical Properties]
Pale Brown Solid | [Uses]
Quinacetol (cas# 2598-31-4) is a compound useful in organic synthesis. | [Production Methods]
Quinacetol was manufactured through a straightforward salt formation step built on the prior synthesis of quinacetol. Commercial producers first generated the quinolinium base by quaternising quinoline with ethylene oxide or ethylene chlorohydrin under controlled conditions, then converting the resulting hydroxyethyl quinolinium intermediate into the acetate (quinacetol). | [Mechanism of action]
Quinoline fungicides tend to act by disrupting fungal metabolism, often targeting nucleic acid biosynthesis or cell membrane integrity | [Pesticide Type]
Fungicide |
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