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7-METHOXY-ISOQUINOLINE

Basic information Uses Safety Supplier Related

7-METHOXY-ISOQUINOLINE Basic information

Product Name:
7-METHOXY-ISOQUINOLINE
Synonyms:
  • 7-Methoxyisoquinoline 96%
  • 7-METHOXY-ISOQUINOLINE
  • 7-Methoxy-2-azanaphthalene
  • Isoquinoline, 7-methoxy-
  • 7-METHOXY-ISOQUINOLINE ISO 9001:2015 REACH
  • 7-Methoxyisoquinoline - [M9820]
CAS:
39989-39-4
MF:
C10H9NO
MW:
159.18
Product Categories:
  • blocks
  • Heterocycles
  • Quinolines
  • Quinoline&Isoquinoline
Mol File:
39989-39-4.mol
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7-METHOXY-ISOQUINOLINE Chemical Properties

Melting point:
49°C
Boiling point:
284.68°C (rough estimate)
Density 
1.1202 (rough estimate)
refractive index 
1.6070 (estimate)
storage temp. 
Sealed in dry,Room Temperature
pka
5.54±0.10(Predicted)
Appearance
Off-white to light brown Solid
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22
Hazard Note 
Irritant
HS Code 
2933499090
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7-METHOXY-ISOQUINOLINE Usage And Synthesis

Uses

7-Methoxyisoquinoline is a useful research chemical for organic synthesis and other chemical processes.

Synthesis

591-31-1

22483-09-6

407-25-0

39989-39-4

General steps: 1. dissolve 60.8 mL of 3-methoxybenzaldehyde in 600 mL of toluene and add 81.9 mL of aminoacetaldehyde dimethyl acetal. 2. Install a Dean-Stark manifold and reflux the reaction mixture for 5 hours, followed by cooling to 5 °C. 3. 209 mL of trifluoroacetic anhydride and 185 mL of boron trifluoride ether compound were slowly added dropwise under nitrogen protection, with the rate of dropwise acceleration controlled to maintain the reaction temperature below 10 °C. The reaction temperature was then increased to 10 °C. The reaction temperature was then increased to 10 °C. 4. After the dropwise addition was completed, the reaction mixture was continued to be stirred at room temperature for 3 days. 5. The reaction mixture was slowly poured into ice water, 250 mL of 2N hydrochloric acid was added, and the organic layer was extracted with 1N hydrochloric acid. 6. Combine the aqueous phases and adjust the pH to 9 with concentrated ammonia. 7. extracted the aqueous phase with ethyl acetate, combined the organic phases, dried and concentrated the solvent under reduced pressure. 8. 66.9 g (84% yield) of 7-methoxyisoquinoline was obtained as a light brown oil. EI-MS: 159 (M+).

References

[1] Patent: US6194409, 2001, B1

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