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2-Iodo-4-methoxy-1-nitrobenzene

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2-Iodo-4-methoxy-1-nitrobenzene Basic information

Product Name:
2-Iodo-4-methoxy-1-nitrobenzene
Synonyms:
  • 3-IODO-4-NITROANISOLE
  • 4-NITRO-3-IODOANISOLE
  • 3-Iodo-4-nitroanisole,97%
  • 2-Iodo-4-Methoxy-1-nitrobenzene
  • 3-Iodo-4-nitroanisole, 97% 5GR
  • 2-Iodo-4-methoxy-1-nitrobenzene, 3-Iodo-4-nitrophenyl methyl ether
  • 3-Iodo-4-nitroanisol
  • Benzene, 2-iodo-4-methoxy-1-nitro-
CAS:
214279-40-0
MF:
C7H6INO3
MW:
279.03
Product Categories:
  • Aromatic Ethers
Mol File:
214279-40-0.mol
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2-Iodo-4-methoxy-1-nitrobenzene Chemical Properties

Melting point:
68-73 °C
Boiling point:
352.1±27.0 °C(Predicted)
Density 
1.9259 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
Crystals or Crystalline Powder
color 
Yellow to orange-brown
InChI
InChI=1S/C7H6INO3/c1-12-5-2-3-7(9(10)11)6(8)4-5/h2-4H,1H3
InChIKey
NLTAHTYBZZSCIT-UHFFFAOYSA-N
SMILES
C1([N+]([O-])=O)=CC=C(OC)C=C1I
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36-33-20/21/22
Safety Statements 
36/37-22
HS Code 
29093090

MSDS

  • Language:English Provider:ACROS
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2-Iodo-4-methoxy-1-nitrobenzene Usage And Synthesis

Chemical Properties

yellow to orange-brown crystals or

Synthesis

Silak reaction tube equipped with a magnetic stirrer was charged with 6.2 mg of silver sulfate,21.8 mg of copper acetate, 12.5 mg of 2,9-dimethyl-1,10-o-phenanthroline,39.4 mg of 2-nitro-5-methoxybenzoic acid and 45 mg of sodium iodide4 mL of dimethyl sulfoxide. The reaction was heated at 160 ° C for 24 hours with oxygen. After the reaction, distilled water was added to quench the reaction. Extraction with ethyl acetate 3 times, each time 10mL. The combined organic phases are concentrated; 35.2 mg of 2-Iodo-4-methoxy-1-nitrobenzene was obtained in a yield of 63 percent.

References

[1] Patent: CN107325002, 2017, A. Location in patent: Paragraph 0133
[2] Organic and Biomolecular Chemistry, 2018, vol. 16, # 30, p. 5416 - 5421
[3] Journal of Organic Chemistry, 2016, vol. 81, # 7, p. 2794 - 2803

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