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8-Quinolinecarboxylic acid

Basic information Safety Supplier Related

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
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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)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29334900

MSDS

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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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