Basic information Safety Supplier Related

4-IODO-3-NITROANISOLE

Basic information Safety Supplier Related

4-IODO-3-NITROANISOLE Basic information

Product Name:
4-IODO-3-NITROANISOLE
Synonyms:
  • 1-IODO-4-METHOXY-2-NITROBENZENE
  • 4-IODO-3-NITROANISOLE
  • 4-Iodo-3-Nitroanisole 3-Nitro-4-Iodoanisole
  • 3-Nitro-4-iodoanisol
  • 3-Nitro-4-Iodoanisole
  • 4-IODO-3-NITROANISOLE, 98+%
  • 4-Iodo-3-nitrianisole
  • NSC 158572
CAS:
58755-70-7
MF:
C7H6INO3
MW:
279.03
EINECS:
209-622-9
Product Categories:
  • Aromatic Ethers
Mol File:
58755-70-7.mol
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4-IODO-3-NITROANISOLE Chemical Properties

Melting point:
61-62°C
Boiling point:
173 °C(Press: 0.9 Torr)
Density 
1.893
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
solid
color 
Light brown to brown
Sensitive 
Light Sensitive
BRN 
2365592
CAS DataBase Reference
58755-70-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37
HazardClass 
IRRITANT, LIGHT SENSITIVE
HS Code 
29093090

MSDS

  • Language:English Provider:ALFA
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4-IODO-3-NITROANISOLE Usage And Synthesis

Synthesis

96-96-8

58755-70-7

General procedure for the synthesis of 4-iodo-3-nitroanisole from 2-nitro-4-methoxyaniline: 11.9 mmol of 2-nitro-4-methoxyaniline was dissolved in 20 mL of concentrated sulfuric acid at a mass concentration of 71%. The temperature of the system was lowered to -5°C. 10 mL of 2 mol/L sodium nitrite solution was rapidly added to the reaction system at 0 °C and under vigorous stirring. The reaction was kept at 0°C for 10 minutes. Subsequently, the reaction mixture was poured into 5 mL of 4 mol/L sodium iodide solution at 0 °C and the reaction was continued for 30 min. Upon completion of the reaction, the solid residue was collected by filtration and washed sequentially with 6N hydrochloric acid and water. The crude product was recrystallized by hexane to give a yellow solid A.

References

[1] Patent: CN105669525, 2016, A. Location in patent: Paragraph 0072; 0073; 0082
[2] Synlett, 2016, vol. 27, # 14, p. 2095 - 2100
[3] Synlett, 2005, # 16, p. 2469 - 2472
[4] Journal of Organic Chemistry, 2001, vol. 66, # 13, p. 4525 - 4542
[5] Angewandte Chemie - International Edition, 2011, vol. 50, # 32, p. 7354 - 7358

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