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7-Hydroxyquinoline

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7-Hydroxyquinoline Basic information

Product Name:
7-Hydroxyquinoline
Synonyms:
  • 7-HYDROXYQUINOLINE 99%
  • 1H-Quinolin-7-one
  • 7-Hydroxyquinoline,99%
  • 7-Hydroxyquinoline, 99% 1GR
  • 7-QUINOLINOL HYDRATE
  • 7-Quinolinol (8CI,9CI)
  • CCRIS 4332
  • 7-HYDROXYQUINOLINE
CAS:
580-20-1
MF:
C9H7NO
MW:
145.16
EINECS:
209-457-2
Product Categories:
  • Hydroxyquinolines
  • Quinolines
  • Quinolines, Quinazolines and derivatives
  • Quinoline&Isoquinoline
  • Heterocycles
Mol File:
580-20-1.mol
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7-Hydroxyquinoline Chemical Properties

Melting point:
239-244 °C
Boiling point:
264.27°C (rough estimate)
Density 
1.1555 (rough estimate)
refractive index 
1.4500 (estimate)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
DMSO (Slightly), Methanol (Slightly)
form 
Powder
pka
pK1:5.48(+1);pK2:8.85(0) (20°C)
color 
Beige to pale brown
Water Solubility 
454.3mg/L(20 ºC)
InChI
InChI=1S/C9H7NO/c11-8-4-3-7-2-1-5-10-9(7)6-8/h1-6,11H
InChIKey
XCRPPAPDRUBKRJ-UHFFFAOYSA-N
SMILES
N1C2C(=CC=C(O)C=2)C=CC=1
CAS DataBase Reference
580-20-1(CAS DataBase Reference)
NIST Chemistry Reference
7-Quinolinol(580-20-1)
EPA Substance Registry System
7-Quinolinol (580-20-1)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-20/21/22-22
Safety Statements 
36/37/39-26
RTECS 
VC4160000
HazardClass 
IRRITANT
HS Code 
29334900

MSDS

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7-Hydroxyquinoline Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Definition

ChEBI: A monohydroxyquinoline carrying a hydroxy substituent at position 7.

Synthesis

3054-95-3

591-27-5

580-20-1

The general procedure for the synthesis of 7-hydroxyquinoline from acrolein diethyl acetal and 3-aminophenol was as follows: the reaction was carried out in a Panasonic NN-K5541JF microwave reactor equipped with a magnetic stirring device. The typical operation was as follows: acrolein diethyl acetal (1 mmol), excess 3-aminophenol (4 mmol) and solid catalyst were added to a round bottom flask; subsequently, the mixture was placed in a microwave reactor. The reaction was carried out by continuous microwave radiation under reflux and stirring conditions for 1 to 40 min. Upon completion of the reaction, the products were analyzed and identified using a Varian Saturn 2200/CP-3800 gas chromatography-mass spectrometer (GC-MS) equipped with two CP8944 capillary columns (VF-5, 30 m × 0.25 mm × 0.25 μm).

References

[1] Catalysis Communications, 2018, vol. 115, p. 21 - 25

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