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INDIUM(III) TRIFLUOROMETHANESULFONATE

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INDIUM(III) TRIFLUOROMETHANESULFONATE Basic information

Product Name:
INDIUM(III) TRIFLUOROMETHANESULFONATE
Synonyms:
  • INDIUM(III) TRIFLUOROMETHANESULFONATE
  • INDIUM(III)TRIFLUOROMETHANESULPHONATE
  • INDIUM(III) TRIFLATE
  • INDIUM TRIFLATE
  • INDIUM TRIFLUOROMETHANESULFONATE
  • INDIUM TRIFLUOROMETHANESULPHONATE
  • IndiumtrifluoromethanesulfonateIndiumtriflatepowder
  • Indiumtrifluoromethanesulphonate98%
CAS:
128008-30-0
MF:
C3F9InO9S3
MW:
562.03
Product Categories:
  • Other Metal
  • triflate
  • Catalysis and Inorganic Chemistry
  • Chemical Synthesis
  • triflate,trifluoromethanesulfonate,OTf
  • metal triflate compounds
  • Indium
Mol File:
128008-30-0.mol
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INDIUM(III) TRIFLUOROMETHANESULFONATE Chemical Properties

Melting point:
>300°C
storage temp. 
Inert atmosphere,Room Temperature
solubility 
Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form 
Powder and Granules
color 
Off-white
Water Solubility 
Slightly soluble in hydrocarbons and diethyl ether. Insoluble in water
Sensitive 
Hygroscopic
Stability:
hygroscopic
InChIKey
UCYRAEIHXSVXPV-UHFFFAOYSA-K
CAS DataBase Reference
128008-30-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,C
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
UN3261
WGK Germany 
3
3-10
Hazard Note 
Corrosive/Hygroscopic
HazardClass 
8
PackingGroup 
II
HS Code 
29310099

MSDS

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INDIUM(III) TRIFLUOROMETHANESULFONATE Usage And Synthesis

Chemical Properties

Off-white powder and granules

Uses

Indium(III) trifluoromethanesulfonate is used as a Lewis acid catalyst in organic synthesis and as a co-catalyst in organometallic catalysis. It is also used as a reactant in the preparation of stable indium bacteriochlorins and decahydroquinoline-type toxins through intramolecular hetero Diels-Alder reactions. Further, it is used in the synthesis of benzoxazoles through cyclocondensations.

Uses

Reactant or reagent involved in:

  • Synthesis of stable indium bacteriochlorins
  • Studying basicities of phosphoryl compounds toward triflates Lewis acids
  • Preparation of decahydroquinoline-type toxins via intramolecular hetero Diels-Alder reactions

Catalyst for synthesis of benzoxazoles via cyclocondensations

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