Basic information Safety Supplier Related

7-Bromoquinolin-8-ol

Basic information Safety Supplier Related

7-Bromoquinolin-8-ol Basic information

Product Name:
7-Bromoquinolin-8-ol
Synonyms:
  • 7-Bromoquinolin-8-ol
  • 7-BroMo-8-hydroxyquinoline
  • 7-BroMo-8-hydroxyquinoline 97%
  • 7-bromo-8-Quinolinol
  • 8-Quinolinol, 7-bromo-
  • 7-bromo-8-hydroxyquinolinol
CAS:
13019-32-4
MF:
C9H6BrNO
MW:
224.05
Mol File:
13019-32-4.mol
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7-Bromoquinolin-8-ol Chemical Properties

Melting point:
138-143 °C
Boiling point:
327.9±22.0 °C(Predicted)
Density 
1.705±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
2.43±0.50(Predicted)
form 
powder
InChI
InChI=1S/C9H6BrNO/c10-7-4-3-6-2-1-5-11-8(6)9(7)12/h1-5,12H
InChIKey
ICKPMTNGWVNOGC-UHFFFAOYSA-N
SMILES
N1C2C(=CC=C(Br)C=2O)C=CC=1
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-41
Safety Statements 
26
WGK Germany 
1
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7-Bromoquinolin-8-ol Usage And Synthesis

Synthesis

148-24-3

521-74-4

13019-32-4

The general procedure for the synthesis of 5,7-dibromo-8-hydroxyquinoline and 7-bromo-8-hydroxyquinoline from 8-hydroxyquinoline was as follows: bromination was carried out according to the method described in the literature [19]. This was done as follows: 8-hydroxyquinoline (2 mmol, 1 eq.) was dissolved in distilled CHCl3 (15 mL) at room temperature and protected from light, followed by the slow addition of different equivalents of molecular bromine (dissolved in CHCl3) over a period of 10 min. The reaction mixture was stirred continuously for 2 days, during which the progress of the reaction was monitored by TLC. Upon completion of the reaction, the organic layer was washed with 5% NaHCO3 solution (3 x 20 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. Finally, the target product was separated by alumina column chromatography with ethyl acetate/hexane (1:5, 150 mL) as eluent.

References

[1] Letters in Drug Design and Discovery, 2017, vol. 14, # 12, p. 1415 - 1424

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