Chemical Property of Indium(III) trifluoromethanesulfonate
Chemical Property:
- Appearance/Colour:Off-white powder and granules
- Vapor Pressure:1.14mmHg at 25°C
- Boiling Point:162 °C at 760 mmHg
- PSA：196.74000
- LogP:3.39660
- Storage Temp.:Inert atmosphere,Room Temperature
- Sensitive.:Hygroscopic
- Solubility.:Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
- Water Solubility.:Slightly soluble in hydrocarbons and diethyl ether. Insoluble in water
- Hydrogen Bond Donor Count:0
- Hydrogen Bond Acceptor Count:18
- Rotatable Bond Count:0
- Exact Mass:561.7599523
- Heavy Atom Count:25
- Complexity:145
- Purity/Quality:
-
99% *data from raw suppliers
Indium(III) trifluoromethanesulfonate
*data from reagent suppliers
Safty Information:
- Pictogram(s):
Xi, 
C
- Hazard Codes:Xi,C
- Statements:
36/37/38
- Safety Statements:
26-36
- MSDS Files:
-
SDS file from LookChem
Useful:
- Canonical SMILES:C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].C(F)(F)(F)S(=O)(=O)[O-].[In+3]
-
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. Reactant or reagent involved in:Synthesis of stable indium bacteriochlorinsStudying basicities of phosphoryl compounds toward triflates Lewis acidsPreparation of decahydroquinoline-type toxins via intramolecular hetero Diels-Alder reactionsCatalyst for synthesis of benzoxazoles via cyclocondensations
