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1-IODO-3,4-METHYLENEDIOXYBENZENE

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1-IODO-3,4-METHYLENEDIOXYBENZENE Basic information

Product Name:
1-IODO-3,4-METHYLENEDIOXYBENZENE
Synonyms:
  • 5-IODO-1,3-BENZODIOXOLE
  • 1-IODO-3,4-METHYLENEDIOXYBENZENE
  • 5-Iodo-2-methylbenzotrifluoride
  • 1-IODO-3,4-METHYLENEDIOXYBENZENE 99%
  • 5-iodo-2H-1,3-benzodioxole
  • 3,4-Methylenedioxyiodobenzene
  • 4-Iodo-1,2-(Methylenedioxy)benzene
  • 5-Iodobenzo[d][1,3]dioxole
CAS:
5876-51-7
MF:
C7H5IO2
MW:
248.02
Product Categories:
  • Aromatics
  • Heterocycles
  • Intermediates
  • Heterocycles series
  • Iodine Compounds
  • Miscellaneous Compounds
  • Aromatic Hydrocarbons (substituted) & Derivatives
Mol File:
5876-51-7.mol
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1-IODO-3,4-METHYLENEDIOXYBENZENE Chemical Properties

Boiling point:
94 °C
Density 
1,91 g/cm3
Flash point:
111℃
storage temp. 
2-8°C(protect from light)
solubility 
Chloroform, Methanol
form 
Oil
color 
Brown
CAS DataBase Reference
5876-51-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38-52-41-37/38
Safety Statements 
26-36/37/39-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29329990
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1-IODO-3,4-METHYLENEDIOXYBENZENE Usage And Synthesis

Chemical Properties

Brown Oil

Uses

1-Iodo-3,4-methylenedioxybenzene is an iodinated benzodioxole used in the preparation of various biologically active compounds such as the antiviral and antitumor agents.

Synthesis

274-09-9

5876-51-7

N-iodosuccinimide (14.8 g, 66.0 mmol), 1,3-benzodioxole (6.31 mL, 55.0 mmol) and acetic acid (470 mL) were added to a 1 L flask under argon protection. The reaction mixture was stirred at room temperature for 65 hours. Upon completion of the reaction, the acetic acid was removed by distillation under reduced pressure and the residue was neutralized with saturated aqueous sodium bicarbonate solution. Subsequently, aqueous sodium thiosulfate and chloroform were added to the reaction mixture to separate the organic layer. The aqueous layer was further extracted with chloroform. All organic layers were combined, dried with anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography using hexane as eluent to afford 5-iodo-1,3-benzodioxole (11.3 g, 45.7 mmol, 83% yield) in colorless liquid form.

References

[1] Advanced Synthesis and Catalysis, 2004, vol. 346, # 1, p. 77 - 82
[2] Patent: JP2015/163597, 2015, A. Location in patent: Paragraph 0167; 0168
[3] Synthesis, 1995, # 10, p. 1273 - 1277
[4] Catalysis Science and Technology, 2014, vol. 4, # 12, p. 4308 - 4312
[5] Tetrahedron Letters, 1987, vol. 28, # 41, p. 4879 - 4882

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