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5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE

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5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE Basic information

Product Name:
5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE
Synonyms:
  • 5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE
  • 5-Fluoro-2-methoxyisonicotinaldehyde
  • 5-Fluoro-2-methoxypyridine-4-carboxaldehyde
  • 4-PYRIDINECARBOXALDEHYDE, 5-FLUORO-2-METHOXY-
  • 5-fluoro-2-methoxypyridine-4-carbaldehyde
  • 5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE ISO 9001:2015 REACH
  • 5-fluoro-2-methoxy-pyridine-4-carbaldehyde - [F87726]
CAS:
884495-12-9
MF:
C7H6FNO2
MW:
155.13
Product Categories:
  • Boronic Acid
  • Heterocyclic Compounds
Mol File:
884495-12-9.mol
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5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE Chemical Properties

Boiling point:
234℃
Density 
1.266
Flash point:
96℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
Appearance
White to off-white Solid
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Safety Information

HS Code 
2933399990
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5-FLUORO-4-FORMYL-2-METHOXYPYRIDINE Usage And Synthesis

Synthesis

1000895-80-6

884495-12-9

The general procedure for the synthesis of 2-methoxy-5-fluoropyridine-4-carboxaldehyde from (5-fluoro-2-methoxypyridin-4-yl)methanol was as follows: (5-fluoro-2-methoxypyridin-4-yl)methanol (1.40 g, 8.91 mmol) was dissolved in dichloromethane (DCM, 50 mL) with stirring. A dichloromethane (DCM, 70 mL) solution of Dess-Martin periodontane (4.535 g, 10.69 mmol) was slowly added and the reaction mixture continued to be stirred for 1.5 hours at room temperature. After completion of the reaction, the organic layer was washed sequentially with 1 M aqueous sodium hydroxide solution (2 x 75 mL), water (75 mL) and brine, dried over anhydrous magnesium sulfate (MgSO?), filtered and concentrated to afford 2-methoxy-5-fluoropyridine-4-carbaldehyde as a yellow oil (0.481 g, 35% yield).1H NMR (399.902 MHz, CDCl?) δ 3.94 (s, 3H), 7.08-7.11 (m, 1H), 8.20-8.22 (m, 1H), 10.32 (s, 1H).

References

[1] Patent: US2008/4302, 2008, A1. Location in patent: Page/Page column 74

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