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DIPHENYLIODONIUM CHLORIDE

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DIPHENYLIODONIUM CHLORIDE Basic information

Product Name:
DIPHENYLIODONIUM CHLORIDE
Synonyms:
  • DIPHENYLIODONIUM CHLORIDE
  • chlorodiphenyliodonium
  • diphenyl-iodoniuchloride
  • Iodonium,diphenyl-,chloride
  • Diphenyliodinium
  • Iodonium,diphenyl-chloride
  • DIPHENYLIODONIUM CHLORIDE 97%
  • Diphenyliodonium chloride,97%
CAS:
1483-72-3
MF:
C12H10ClI
MW:
316.57
EINECS:
216-049-8
Product Categories:
  • Diphenyliodonium Compounds
  • Hypervalent Iodine Compounds
  • Iodonium Sulfonium & Oxonium Compounds
  • Synthetic Organic Chemistry
  • Hypervalent Iodine
  • Oxidation
  • Synthetic Reagents
Mol File:
1483-72-3.mol
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DIPHENYLIODONIUM CHLORIDE Chemical Properties

Melting point:
233-235 °C (subl.) (lit.)
Density 
1.6151 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
Powder
color 
White to light cream-yellow
Water Solubility 
Soluble in water and methanol.
Sensitive 
Light Sensitive
Merck 
14,7464
BRN 
3574977
InChIKey
RSJLWBUYLGJOBD-UHFFFAOYSA-M
CAS DataBase Reference
1483-72-3(CAS DataBase Reference)
EPA Substance Registry System
Iodonium, diphenyl-, chloride (1483-72-3)
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Safety Information

Hazard Codes 
T,Xi
Risk Statements 
25-36/37/38
Safety Statements 
26-36
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
RTECS 
NN6651666
8
TSCA 
Yes
HazardClass 
6.1
PackingGroup 
III
HS Code 
29319090

MSDS

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DIPHENYLIODONIUM CHLORIDE Usage And Synthesis

Chemical Properties

WHITE TO LIGHT CREAM-YELLOW POWDER

Uses

Diphenyliodonium chloride is used as a reagent for electrophilic phenylation . It is used as a reactant for copper-catalyzed cross coupling reactions of purinesband arylation of anilines. It is involved in the preparation of acetylenic arylselenide and (arylmethylene)oxindoles. Further, it is employed in the preparation of aryl alkynes through Sonogashira coupling reactions.

Uses

Reactant for:

  • Copper-catalyzed cross coupling reactions of purines and diaryliodonium salts
  • Synthesis of acetylenic arylselenides
  • Sonogashira coupling reactions for the preparation of aryl alkynes
  • C-H functionalization for synthesis of (arylmethylene)oxindoles
  • Arylation of anilines
  • Studies on the visible-light photosensitive system-dlourescein yellow-bis(di-Ph iodonium)
  • Investigating the properties of direct and sensitized photolysis of dispersed photoacid generators

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