CAS 128008-30-0 Indium(III) trifluoromethanesulfonate

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

Exact Mass

561.76g/mol

H-Bond Acceptor

Heavy Atom Count

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.

March 28, 2025

Exceptional Catalyst for Advanced Research

Indium(III) trifluoromethanesulfonate is indispensable in our lab for organic synthesis. As a Lewis acid catalyst, it aids in synthesizing stable indium compounds efficiently. Reliable for complex reactions like Diels-Alder, enhancing research productivity significantly.