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Indium(III) trifluoromethanesulfonate

Catalog Number
ACM128008300-2
Product Name
Indium(III) trifluoromethanesulfonate
Structure
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CAS
128008-30-0
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Synonyms
ST24030780; TR-003978; indium trifluoromethanesulphonate; I09-1715; indium (III) trifluoromethanesulfonate; MFCD00144478 (98%); KSC491Q8T; M-8607; ACMC-209bda; Indium trifluoromethanesulfonate;
IUPAC Name
indium(3+);trifluoromethanesulfonate;
Molecular Weight
562.008g/mol
Molecular Formula
C3F9InO9S3;
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];
InChI
InChI=1S/3CHF3O3S.In/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3;
InChI Key
UCYRAEIHXSVXPV-UHFFFAOYSA-K;
Complexity
145
Covalently-Bonded Unit Count
4
Exact Mass
561.76g/mol
H-Bond Acceptor
18
Heavy Atom Count
25
Monoisotopic Mass
561.76g/mol
Topological Polar Surface Area
197A^2
Application
Indium(III) trifluoromethanesulfonate, appearing as an off-white powder and granules, serves a crucial role in various chemical processes. It acts as a Lewis acid catalyst in organic synthesis and functions as a co-catalyst in organometallic catalysis, facilitating numerous intricate reactions. Moreover, it is employed as a reactant in producing stable indium bacteriochlorins and decahydroquinoline-type toxins through intramolecular hetero Diels-Alder reactions. Additionally, it aids in synthesizing benzoxazoles through cyclocondensations. Its utility extends to studying the basicities of phosphoryl compounds toward triflates Lewis acids, making it an essential component in advanced chemical synthesis and research.
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