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2-Quinolinol

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2-Quinolinol Basic information

Product Name:
2-Quinolinol
Synonyms:
  • 2-Oxo-1,2-dihydroquinoline
  • 1,2-Dihydroquinolin-2-one
  • 2-Hydroxyquinoline, 99% 10GR
  • Carbostyril 2-Hydroxyquinoline
  • Quinolin-2-ol, 2-Hydroxy-1-azanaphthalene, Carbostyril
  • 2-quinolinol:2-hydroxyQUINOLINE: carbostyril
  • 2-Quinolinol, Carbostyril
  • 2(1h)-quinolinone
CAS:
59-31-4
MF:
C9H7NO
MW:
145.16
EINECS:
200-420-6
Product Categories:
  • Hydroxyquinolines
  • Quinolines
  • bc0001
Mol File:
59-31-4.mol
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2-Quinolinol Chemical Properties

Melting point:
198-199 °C (lit.)
Boiling point:
264.27°C (rough estimate)
Density 
1.1555 (rough estimate)
refractive index 
1.4500 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
alcohol: soluble(lit.)
form 
Powder
pka
-0.31, 11.76(at 20℃)
color 
White to light purple or purple-brownish
Water Solubility 
1.052g/L(20 ºC)
Merck 
14,1825
BRN 
2855
CAS DataBase Reference
59-31-4(CAS DataBase Reference)
NIST Chemistry Reference
2(1H)-Quinolinone(59-31-4)
EPA Substance Registry System
2(1H)-Quinolinone (59-31-4)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-20/21/22-41-37/38-22
Safety Statements 
26-37/39-36
RIDADR 
2811
WGK Germany 
3
RTECS 
FG7175000
Hazard Note 
Harmful/Irritant
TSCA 
Yes
HS Code 
29334900

MSDS

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2-Quinolinol Usage And Synthesis

Chemical Properties

white to light purple or purple-brownish powder

Uses

2-Hydroxyquinoline was used to obtain the design of the platinum(IV) complexes with intense bands shifted towards longer wavelengths. The Pt(IV) complexes are inert stable prodrugs that were photoactivated to produce Pt(II) species with promising anticancer activity.

Definition

ChEBI: A quinolone that is 1,2-dihydroquinoline substituted by an oxo group at position 2.

Synthesis Reference(s)

Synthesis, p. 739, 1975 DOI: 10.1055/s-1975-23918

General Description

2-Hydroxyquinoline is a specific inhibitor of plaque paraoxonase1 (PON1).

Purification Methods

Crystallise it from MeOH. It has m 200-201o after sublimation in a vacuum. The picrate has m 132o after crystallisation from Et2O. [Gibson et al. J Chem Soc 4340 1955, Beilstein 21 III/IV 1057, 21/8 V 217.]

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