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4-Iodoanisole

4-Iodoanisole (chemical formula: C7H7IO) is an organic compound being soluble in ethanol, ether and chloroform. It has a wide range of medicals industrial applications. For example, it can be used as human and animal nutrition products, antiseptics, disinfectants, pharmaceutical intermediates, polarizing films for liquid crystal display (LCD) chemicals. Its iodine derivatives can also be used as organic building blocks and analytic reagents.

Basic information Description References Safety Related Supplier
4-Iodoanisole Basic information
4-Iodoanisole Chemical Properties
  • Melting point:50-53 °C(lit.)
  • Boiling point:237 °C726 mm Hg(lit.)
  • Density 1.7904 (estimate)
  • Flash point:>230 °F
  • storage temp. Keep in dark place,Sealed in dry,Room Temperature
  • solubility Soluble in ethanol, ether, chloroform.
  • form Crystalline Powder and Chunks
  • color Off-white to brown
  • Sensitive Light Sensitive
  • BRN 1906692
  • InChIKeySYSZENVIJHPFNL-UHFFFAOYSA-N
  • CAS DataBase Reference696-62-8(CAS DataBase Reference)
  • NIST Chemistry ReferenceBenzene, 1-iodo-4-methoxy-(696-62-8)
  • EPA Substance Registry SystemBenzene, 1-iodo-4-methoxy- (696-62-8)
Safety Information
  • Hazard Codes Xi,Xn
  • Risk Statements 36/37/38
  • Safety Statements 26-36-24/25
  • WGK Germany 3
  • 8
  • TSCA Yes
  • HS Code 29093090
MSDS
4-Iodoanisole Usage And Synthesis
  • Description4-Iodoanisole (chemical formula: C7H7IO) is an organic compound being soluble in ethanol, ether and chloroform. It has a wide range of medicals industrial applications. For example, it can be used as human and animal nutrition products, antiseptics, disinfectants, pharmaceutical intermediates, polarizing films for liquid crystal display (LCD) chemicals. Its iodine derivatives can also be used as organic building blocks and analytic reagents.
  • Referenceshttps://www.fishersci.pt/shop/products/4-iodoanisole-98-7/11480113
  • Chemical Propertiesoff-white to brown crystalline powder and chunks
  • Usessuzuki reaction
  • UsesIntermediates of Liquid Crystals
  • Synthesis Reference(s)The Journal of Organic Chemistry, 58, p. 2058, 1993 DOI: 10.1021/jo00060a020
    Tetrahedron Letters, 27, p. 3497, 1986 DOI: 10.1016/S0040-4039(00)84832-7
  • Purification MethodsCrystallise 4-iodoanisole from aqueous EtOH and/or distil it under vacuum. [Beilstein 6 H 208, 6 I 109, 6 II 199, 6 III 744, 6 IV 1075.]
4-Iodoanisole Preparation Products And Raw materials
4-Iodoanisole(696-62-8)Related Product Information
4-IodoanisoleSupplierMore
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