8-Quinolinecarboxylic acid
8-Quinolinecarboxylic acid Basic information
- Product Name:
- 8-Quinolinecarboxylic acid
- Synonyms:
-
- RARECHEM AL BE 0482
- QUINOLINE-8-CARBOXYLIC ACID
- 8-QUINOLINECARBOXYLIC ACID
- AKOS BBS-00005343
- QUINOLINE-8-CARBOXYLIC ACID, 98+%
- 8-Quinolinecarboxylic
- 8-quinlinecarboxylic acid
- 8-Carboxyquinoline
- CAS:
- 86-59-9
- MF:
- C10H7NO2
- MW:
- 173.17
- EINECS:
- 632-930-3
- Product Categories:
-
- Building Blocks
- Heterocyclic Building Blocks
- Quinolines, Quinazolines and derivatives
- Quinolines
- Quinolinecarboxylic Acids, etc.
- quinoline
- Quinoline Derivertives
- Mol File:
- 86-59-9.mol
8-Quinolinecarboxylic acid Chemical Properties
- 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
- pka
- 1.82(at 25℃)
- form
- Crystalline Powder
- color
- Light brown
- Water Solubility
- Insoluble
- Merck
- 14,8070
- BRN
- 19176
- InChIKey
- QRDZFPUVLYEQTA-UHFFFAOYSA-N
- CAS DataBase Reference
- 86-59-9(CAS DataBase Reference)
MSDS
- Language:English Provider:8-Quinolinecarboxylic acid
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
8-Quinolinecarboxylic acid Usage And Synthesis
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 and 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
- 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.]
8-Quinolinecarboxylic acid Preparation Products And Raw materials
Preparation Products
Raw materials
8-Quinolinecarboxylic acidSupplier
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8-Quinolinecarboxylic acid(86-59-9)Related Product Information
- Ethoxyquin
- Quinolinic acid
- Ethyl 2-(Chlorosulfonyl)acetate
- 8-Hydroxyquinoline
- 5,6,7,8-TETRAHYDROISOQUINOLINE
- Citric acid
- Quinclorac
- 1,2,3,4-TETRAHYDROISOQUINOLINE
- Quinaldic acid
- Quinhydrone
- Glycine
- Folic acid
- Isoquinoline
- 8-Quinolinemethanol
- Ascoric Acid
- 7-CHLORO-1,4-DIHYDRO-L-ETHYL-6-FLUORO-4-OXO-3-QUINOLINECARBOXYLIC ACID
- N-CBZ-3,4-DIHYDRO-1H-ISOQUINOLINECARBOXYLIC ACID
- Garenoxacin