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Iodobenzene dichloride information


Iodobenzene dichloride[1]
Names
Preferred IUPAC name
Dichloro(phenyl)-λ3-iodane
Other names
Iodosobenzene dichloride; Phenyliodine(III) dichloride; Phenyliodo dichloride; Phenyliodoso chloride; Phenylchloroiodonium chloride; Dichloroiodobenzene; Iododichlorobenzene
Identifiers
CAS Number
  • 932-72-9 checkY
3D model (JSmol)
  • Interactive image
Abbreviations IBD
ChemSpider
  • 254526
PubChem CID
  • 13166207
UNII
  • 0IJ835PQB7 checkY
CompTox Dashboard (EPA)
  • DTXSID50302248 Edit this at Wikidata
SMILES
  • Cl[I](c1ccccc1)Cl
Properties
Chemical formula
C6H5Cl2I
Molar mass 274.91 g·mol−1
Appearance Yellow solid
Density 2.2 g/cm3
Melting point 115 to 120 °C (239 to 248 °F; 388 to 393 K) (decomposes)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Iodobenzene dichloride (PhICl2) is a complex of iodobenzene with chlorine. As a reagent for organic chemistry, it is used as an oxidant and chlorinating agent.

  1. ^ Phenyliodine(III) Dichloride, David W. Knight and Glen A. Russell, in Encyclopedia of Reagents for Organic Synthesis, 2001, John Wiley & Sons, Ltd doi:10.1002/047084289X.rp071

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Iodobenzene dichloride

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Iodobenzene dichloride (PhICl2) is a complex of iodobenzene with chlorine. As a reagent for organic chemistry, it is used as an oxidant and chlorinating...

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Iodobenzene

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synthon. Iodobenzene reacts with chlorine to give the complex, iodobenzene dichloride, which is used as a solid source of chlorine. Iodobenzene can also...

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Triphenylphosphine dichloride

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stoichiometry. Ph3PCl2 can also be obtained by the reaction of iodobenzene dichloride (PhICl2) and triphenylphosphine. Alternatively, Ph3PCl2 can be obtained...

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IBD

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beta decay, a nuclear reaction commonly used in neutrino detectors Iodobenzene dichloride, a reagent used in organic chemistry Ion beam deposition International...

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Iodine

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common reagent for the oxidation of alcohols to aldehydes, and iodobenzene dichloride (PhICl2), used for the selective chlorination of alkenes and alkynes...

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Iodine compounds

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common reagent for the oxidation of alcohols to aldehydes, and iodobenzene dichloride (PhICl2), used for the selective chlorination of alkenes and alkynes...

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Hypervalent organoiodine compounds

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the first hypervalent iodine compound, iodobenzene dichloride (PhICl2), by passing chlorine gas through iodobenzene in a cooled solution of chloroform: PhI...

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Chlorobenzene

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presence of a catalytic amount of Lewis acid such as ferric chloride, sulfur dichloride, and anhydrous aluminium chloride: The catalyst enhances the electrophilicity...

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Sonogashira coupling

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the symmetrical Sonogashira coupling of two equivalents of 1-bromo-4-iodobenzene with trimethylsilylacetylene (with the trimethylsilyl group removed in-situ)...

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List of compounds with carbon number 10

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fluoridamid 47000-92-0 C10H11F5OSi ethanol dmpfps 71338-73-3 C10H11IO4 iodobenzene diacetate 3240-34-4 C10H11N benzenebutanenitrile 2046-18-6 C10H11NO cyclopropiophenone...

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List of compounds with carbon number 6

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C6H4BrCl3Si bromophenyltrichlorosilane 27752-77-8 C6H4BrI 1-Bromo-4-iodobenzene 589-87-7 C6H4F6O2 hexafluoroisopropyl acrylate 2160-89-6 C6H4N cyanocyclopentadienyl...

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Glossary of chemical formulae

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carbonate 534-16-7 Ag2C2O4 silver oxalate 533-51-7 Ag2Cl2 silver(II) dichloride 75763-82-5 Ag2CrO4 silver chromate 7784-01-2 Ag2Cr2O7 silver dichromate...

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