assay
98%
mp
183-185 °C (lit.)
functional group
carboxylic acid
SMILES string
OC(=O)c1cccc2cccnc12
InChI
1S/C10H7NO2/c12-10(13)8-5-1-3-7-4-2-6-11-9(7)8/h1-6H,(H,12,13)
InChI key
QRDZFPUVLYEQTA-UHFFFAOYSA-N
General description
Herbicide 8-quinolinecarboxylic acid and its removal from aqueous solution using sodium montmorillonite, acidic montmorillonite and organo-acidic montmorillonite has been reported.
Application
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Chiral quinolinyl-oxazolines as ligands for copper (I)-catalyzed asymmetric cyclopropanation.
Wu X-Y, et al.
Tetrahedron Asymmetry, 9(23), 4143-4150 (1998)
S López-Bernabeu et al.
Chemosphere, 144, 982-988 (2015-10-05)
The effect of the electrochemical treatment (potentiostatic treatment in a filter-press electrochemical cell) on the adsorption capacity of an activated carbon cloth (ACC) was analyzed in relation with the removal of 8-quinolinecarboxylic acid pollutant from water. The adsorption capacity of
Chiral 1, 2, 3, 4-tetrahydroquinolinyl-oxazoline ligands for Ru-catalyzed asymmetric transfer hydrogenation of ketones.
Zhou Y-B, et al.
Tetrahedron Asymmetry, 13(5), 469-473 (2002)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 367796-250MG | 04061833482421 |