8-????????
|
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8-???????? ??
- ???
- 183-185 °C (lit.)
- ?? ?
- 303.81°C (rough estimate)
- ??
- 1.2427 (rough estimate)
- ???
- 1.5200 (estimate)
- ?? ??
- Sealed in dry,Room Temperature
- ??? ??
- ??? ??
- ?? ?? (pKa)
- 1.82(at 25℃)
- ??
- ?? ??
- ???
- ???
- Merck
- 14,8070
- BRN
- 19176
- InChI
- InChI=1S/C10H7NO2/c12-10(13)8-5-1-3-7-4-2-6-11-9(7)8/h1-6H,(H,12,13)
- InChIKey
- QRDZFPUVLYEQTA-UHFFFAOYSA-N
- SMILES
- N1C2C(=CC=CC=2C(O)=O)C=CC=1
- CAS ??????
- 86-59-9(CAS DataBase Reference)
??
- ?? ? ?? ??
- ?? ? ???? ?? (GHS)
| ??? ?? | Xi | ||
|---|---|---|---|
| ?? ???? ?? | 36/37/38 | ||
| ????? | 26-37/39 | ||
| WGK ?? | 3 | ||
| ?? ?? | IRRITANT | ||
| HS ?? | 29334900 | ||
| ???? ??? | 11 - Combustible Solids | ||
| Hazard Classifications | Eye Irrit. 2 Skin Irrit. 2 STOT SE 3 |
8-???????? C??? ??, ??, ??
??? ??
white to light yellow crystal powder??
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.?? ??
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.]8-???????? ?? ?? ? ???
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8-???????? ?? ??
???( 223)?? ??
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|---|---|---|---|---|---|
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