Indium(III) trifluoromethanesulfonate

Base Information

• Chemical Name: Indium(III) trifluoromethanesulfonate
• CAS No.: 128008-30-0
• Molecular Formula: C3F9InO9S3
• Molecular Weight: 562.03
• Hs Code.: 29310099
• European Community (EC) Number: 628-947-0
• DSSTox Substance ID: DTXSID70370444
• Nikkaji Number: J1.142.389B
• Mol file: 128008-30-0.mol

Synonyms:Indium(III) trifluoromethanesulfonate

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