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4-HYDROXY-1-METHYL-2-QUINOLONE

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4-HYDROXY-1-METHYL-2-QUINOLONE Basic information

Product Name:
4-HYDROXY-1-METHYL-2-QUINOLONE
Synonyms:
  • AURORA KA-2363
  • 4-HYDROXY-1-METHYL-2-QUINOLONE
  • 4-HYDROXY-1-METHYL-1,2-DIHYDROQUINOLIN-2-ONE
  • 4-HYDROXY-1-METHYL-1H-QUINOLIN-2-ONE
  • 4-HYDROXY-1-METHYL-2(1H)-QUINOLONE
  • 4-HYDROXY-N-METHYL-2-QUINOLONE
  • 4-Hydroxy-1-methyl-2(1H)-quinolone 98%
  • 4-hydroxy-1-methylquinolin-2-one
CAS:
1677-46-9
MF:
C10H9NO2
MW:
175.18
EINECS:
216-830-3
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Intermediates of Dyes and Pigments
  • Quinolines
Mol File:
1677-46-9.mol
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4-HYDROXY-1-METHYL-2-QUINOLONE Chemical Properties

Melting point:
269-271 °C (lit.)
Boiling point:
306.47°C (rough estimate)
Density 
1.326
refractive index 
1.5060 (estimate)
pka
4.50±1.00(Predicted)
form 
powder to crystal
color 
Light yellow to Brown to Dark green
CAS DataBase Reference
1677-46-9(CAS DataBase Reference)
EPA Substance Registry System
2(1H)-Quinolinone, 4-hydroxy-1-methyl- (1677-46-9)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
FG7350000
Hazard Note 
Irritant
HS Code 
2933499090
Toxicity
mouse,LD50,intravenous,180mg/kg (180mg/kg),U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#01354,

MSDS

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4-HYDROXY-1-METHYL-2-QUINOLONE Usage And Synthesis

Uses

4-Hydroxy-1-methyl-2(1H)-quinolone was used as nucleophile in electrochemical oxidation of catechols and the reaction was studied by cyclic voltammetry and controlled-potential coulometry. It was used in ceric ammonium nitrate-mediated oxidative cycloaddition of 1,3-dicarbonyls to conjugated compounds to yield substituted dihydrofurans, dihydrofurocoumarins, dihydrofuroquinolinones and dihydrofurophenalenones. It was used in the synthesis of :

  • 3-(4-methoxybenzyl)-4-hydroxy-1-methylquinolinone
  • 3-(benzo[d][1,3]dioxol-5-ylmethyl)-4-hydroxy-1-methylquinolin-2(1H)-one
  • 3-(4-chlorobenzyl)-4-hydroxy-1-methylquinolin-2(1H)-one
  • 3,3′-bis(4-chlorobenzylidene)-1,10-methylquinolin-2,20-(1H)-one

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