Basic information Safety Supplier Related

1-CHLORO-5-FLUORO-2-METHOXY-4-NITROBENZENE

Basic information Safety Supplier Related

1-CHLORO-5-FLUORO-2-METHOXY-4-NITROBENZENE Basic information

Product Name:
1-CHLORO-5-FLUORO-2-METHOXY-4-NITROBENZENE
Synonyms:
  • 2-CHLORO-4-FLUORO-5-NITROANISOLE
  • 1-CHLORO-5-FLUORO-2-METHOXY-4-NITROBENZENE
  • 4-Chloro-2-fluoro-5-methoxy-1-nitrobenzene
  • 1-Chloro-5-fluoro-2-methoxy-4-nitrobenzene, 2-Chloro-4-fluoro-5-nitrophenyl methyl ether
  • uoro-2-methoxy-4-nitrobenzene
  • Benzene, 1-chloro-5-fluoro-2-methoxy-4-nitro-
CAS:
84478-76-2
MF:
C7H5ClFNO3
MW:
205.57
Mol File:
84478-76-2.mol
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1-CHLORO-5-FLUORO-2-METHOXY-4-NITROBENZENE Chemical Properties

Melting point:
72-75°C
Boiling point:
307.9±37.0 °C(Predicted)
Density 
1.453
storage temp. 
Sealed in dry,Room Temperature
form 
Solid
Appearance
White to off-white Solid
CAS DataBase Reference
84478-76-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,C
Risk Statements 
34
Safety Statements 
26-36/37/39-45
HazardClass 
IRRITANT
HS Code 
2909309090
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1-CHLORO-5-FLUORO-2-METHOXY-4-NITROBENZENE Usage And Synthesis

Synthesis

84478-75-1

74-88-4

84478-76-2

Potassium carbonate (18 g, 131 mmol) and iodomethane (8.0 mL, 131 mmol) were added to a solution of 2-chloro-4-fluoro-5-nitrophenol (5.0 g, 26.1 mmol) in acetone (100 mL) and stirred at room temperature. The reaction mixture was stirred at room temperature for 2 h. The progress of the reaction was monitored by thin layer chromatography (TLC). After completion of the reaction, the solvent was removed by evaporation under reduced pressure. The residue was diluted with distilled water (100 mL) and extracted with ethyl acetate (3 x 100 mL). The organic layers were combined, washed sequentially with distilled water (100 mL) and saturated saline (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 2-chloro-4-fluoro-5-nitroanisole as a yellow solid. Yield: 5.0 g (93%). 1H NMR (400 MHz, DMSO-d6): δ 7.94-7.97 (m, 1H), 7.81-7.83 (m, 1H), 3.95 (s, 3H).

References

[1] Patent: WO2018/37223, 2018, A1. Location in patent: Page/Page column 206; 207
[2] Patent: US5136868, 1992, A
[3] Patent: US4427438, 1984, A
[4] Patent: US2004/162282, 2004, A1
[5] Patent: US2009/143367, 2009, A1. Location in patent: Page/Page column 37-38

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