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4-Fluoroisoquinoline

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4-Fluoroisoquinoline Basic information

Product Name:
4-Fluoroisoquinoline
Synonyms:
  • 4-fluoroisoquinoline sulfate
  • Isoquinoline, 4-fluoro-
  • 4-Fluoroisoquinoline 95+%
  • 4-Fluoroisoquinoline ISO 9001:2015 REACH
  • 4-FLUOROISOQUINOLINE
  • 4-Floro isoquinoli11e
CAS:
394-67-2
MF:
C9H6FN
MW:
147.15
Mol File:
394-67-2.mol
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4-Fluoroisoquinoline Chemical Properties

Melting point:
34 °C
Boiling point:
240℃
Density 
1.216
refractive index 
1.5914
Flash point:
99℃
storage temp. 
2-8°C
form 
powder to lump
pka
3.45±0.10(Predicted)
color 
White to Light yellow
InChI
InChI=1S/C9H6FN/c10-9-6-11-5-7-3-1-2-4-8(7)9/h1-6H
InChIKey
VFFQGPWQVYUFLV-UHFFFAOYSA-N
SMILES
C1C2=C(C=CC=C2)C(F)=CN=1
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Safety Information

HS Code 
2933491090
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4-Fluoroisoquinoline Usage And Synthesis

Uses

4-fluoroisoquinoline is a useful research chemical.

Synthesis

1532-97-4

394-67-2

General procedure for the synthesis of 4-fluoroisoquinoline from 4-bromoisoquinoline: A solution of 4-bromoisoquinoline (20 g, 96.6 mmol) dissolved in 144 mL of THF was added slowly and dropwise to a 760 mL THF solution containing n-butyllithium (133 mL, 332.5 mmol, 2.5 M in THF) at -65 °C. After the dropwise addition was completed, the reaction mixture was continued to be stirred at -65 °C for 30 min. Subsequently, a solution of N-fluorobenzenesulfonimide (66.68 g, 211.7 mmol) dissolved in 216 mL THF was added dropwise at the same temperature. After addition, the reaction was maintained at -65 °C for 1 hour. Upon completion of the reaction, the mixture was slowly warmed to room temperature and the reaction was quenched by the addition of 300 mL of saturated aqueous ammonium chloride. The reaction mixture was extracted with ethyl acetate (300 mL x 3), and the combined organic phases were washed with 300 mL of saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (elution gradient: 0-100% ethyl acetate/petroleum ether) to afford 4-fluoroisoquinoline (8.5 g, red oil, yield: 60%).

References

[1] Journal of the American Chemical Society, 2014, vol. 136, # 10, p. 3792 - 3795
[2] Patent: US2017/37050, 2017, A1. Location in patent: Paragraph 0301; 0302
[3] Patent: US2007/179127, 2007, A1. Location in patent: Page/Page column 47-48
[4] Patent: US2009/48223, 2009, A1. Location in patent: Page/Page column 101
[5] Patent: US2010/93789, 2010, A1. Location in patent: Page/Page column 46

4-FluoroisoquinolineSupplier

AstaTech (Chengdu) Pharma. Co., Ltd. Gold
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Nanjing Chemlin Chemical Co., Ltd
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Chembon Pharmaceutical Co., Ltd.
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TOKYO CHEMICAL INDUSTRY CO., LTD.
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03-36680489
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