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6-BROMO-3-CHLOROISOQUINOLINE

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6-BROMO-3-CHLOROISOQUINOLINE Basic information

Product Name:
6-BROMO-3-CHLOROISOQUINOLINE
Synonyms:
  • 6-BROMO-3-CHLOROISOQUINOLINE
  • 6-Bromo-3-chloro-2-azanaphthalene
  • 6-bromanyl-3-chloranyl-isoquinoline
  • Isoquinoline, 6-bromo-3-chloro-
  • 6-BROMO-3-CHLOROISOQUINOLINE ISO 9001:2015 REACH
CAS:
552331-06-3
MF:
C9H5BrClN
MW:
242.5
Product Categories:
  • Building Blocks
  • Isoquinoline
Mol File:
552331-06-3.mol
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6-BROMO-3-CHLOROISOQUINOLINE Chemical Properties

Boiling point:
349.5±22.0 °C(Predicted)
Density 
1.673±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
1.28±0.38(Predicted)
form 
solid
color 
Pale yellow
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933499090
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6-BROMO-3-CHLOROISOQUINOLINE Usage And Synthesis

Synthesis

552331-05-2

552331-06-3

General procedure for the synthesis of 6-bromo-3-chloroisoquinoline from 6-bromo-1,3-dichloroisoquinoline: a mixture of 6-bromo-1,3-dichloroisoquinoline (1.8 g, 6.5 mmol), red phosphorus (0.48 g, 15.5 mmol), and hydriodic acid (3 ml, 48%) in acetic acid (20 ml) was heated and refluxed for 8 hours. After completion of the reaction, it was filtered while hot and the filtrate was concentrated under reduced pressure. The concentrated residue was alkalized by addition of sodium hydroxide solution and subsequently extracted with ethyl acetate (200 mL). The organic phase was washed with saturated saline, dried over anhydrous magnesium sulfate, filtered and concentrated. The concentrate was purified by silica gel fast column chromatography to afford 6-bromo-3-chloroisoquinoline (0.81 g, 50% yield) using 30% ethyl acetate/hexane as eluent. Mass spectrum (DCI/NH3) m/e 244 (M+H)+.

References

[1] Patent: US2003/187026, 2003, A1
[2] Patent: US2003/199511, 2003, A1. Location in patent: Page/Page column 34-35

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