| Identification | More | [Name]
8-Quinolinecarboxylic acid | [CAS]
86-59-9 | [Synonyms]
8-QUINOLINECARBOXYLIC ACID
AKOS BBS-00005343
QUINOLINE-8-CARBOXYLIC ACID
RARECHEM AL BE 0482
QUINOLINE-8-CARBOXYLIC ACID, 98+%
8-Quinolinecarboxylic
8-quinlinecarboxylic acid
8-Quinolinecarboxylic acid ,98% | [EINECS(EC#)]
632-930-3 | [Molecular Formula]
C10H7NO2 | [MDL Number]
MFCD00047619 | [Molecular Weight]
173.17 | [MOL File]
86-59-9.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
183-185 °C (lit.) | [Boiling point ]
303.81°C (rough estimate) | [density ]
1.2427 (rough estimate) | [refractive index ]
1.5200 (estimate) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
Crystalline Powder | [pka]
1.82(at 25℃) | [color ]
Light brown | [Water Solubility ]
Insoluble | [Detection Methods]
HPLC | [Merck ]
14,8070 | [BRN ]
19176 | [InChIKey]
QRDZFPUVLYEQTA-UHFFFAOYSA-N | [CAS DataBase Reference]
86-59-9(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection . | [WGK Germany ]
3
| [HazardClass ]
IRRITANT | [HS Code ]
29334900 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
8-Quinolinecarboxylic acid may be used in the synthesis of:
- novel oxorhenium(V) complexes incorporating quinoline and isoquinoline carboxylic acid derivatives
- chiral 1,2,3,4-tetrahydroquinolinyl-oxazoline compounds, used as ligands for Ru-catalyzed asymmetric transfer hydrogenation of ketones
- chiral quinolinyl-oxazoline compounds, used as ligands for Cu(II) catalyzed asymmetric cyclopropanation
| [Uses]
8-Quinolinecarboxylic acid may be used in the synthesis of novel oxorhenium(V) complexes incorporating quinoline and isoquinoline carboxylic acid derivatives, chiral 1,2,3,4-tetrahydroquinolinyl-oxazoline compounds, used as ligands for Ru-catalyzed asymmetric transfer hydrogenation of ketones and chiral quinolinyl-oxazoline compounds, used as ligands for Cu(II) catalyzed asymmetric cyclopropanation. | [General Description]
Herbicide 8-quinolinecarboxylic acid and its removal from aqueous solution using sodium montmorillonite, acidic montmorillonite and organo-acidic montmorillonite has been reported. | [Purification Methods]
Crystallise the acid from water, aqueous EtOH, EtOH or *C6H6. The ethyl ester has m 45o and b 194-197o/13mm. [Beilstein 22 H 81, 22 III/IV 1200, 22/3 V 217.] |
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