CAS 128008-30-0
:Trifluormethansulfonat von Indium
- Indium(III) trifluoromethanesulphonate
- IndiumtrifluoromethanesulfonateIndiumtriflatepowder
- Indium(III) triflate
- Indium(III) trifluoromethanesulfonate
- Indium Tris(Trifluoromethanesulfonate)
- INDIUM TRIFLUOROMETHANESULFONATE
- Indium(III)trifluoromethanesulfonate,99%(Indiumtriflate)
- Indium trifluoromethanesulphonate 98%
- INDIUM TRIFLATE
- Indium(III) trifluoromethanesulphonate, 98+%
- Indium(III) trifluoromethanesulfonate, 99% min
- INDIUM TRIFLUOROMETHANESULPHONATE
- Indiumtrifluoromethanesulphonate98%
- INDIUM(III) TRIFLUOROMETHANESULFONATE (INDIUM TRIFLATE)
- Weitere Synonyme anzeigen
Indium(III) trifluoromethanesulfonate, 99% min
CAS: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-Alde
Formel:C3F9InO9S3Reinheit:99%Molekulargewicht:562.01Indium(III) trifluoromethanesulfonate, 99% (Indium triflate)
CAS:Indium(III) trifluoromethanesulfonate, 99% (Indium triflate)
Formel:In(CF3SO3)3Reinheit:99%Farbe und Form:white pwdr.Molekulargewicht:562.02Indium(lll) trifluoromethanesulfonate
CAS:Formel:In(CF3SO3)3Reinheit:≥ 99.0%Farbe und Form:White to off-white crystalline powder or crystalsMolekulargewicht:562.02Indium trifluoromethanesulphonate
CAS:Indium trifluoromethanesulphonateReinheit:95%Farbe und Form:PowderMolekulargewicht:562.03g/molIndium(III) trifluoromethanesulfonate
CAS:Indium trifluoromethanesulfonate is a reactive, c1-c4 haloalkyl. It has been used as a reagent for the synthesis of serine protease inhibitors. Indium trifluoromethanesulfonate reacts with unsaturated ketones to form x-ray absorption products, which can be analyzed by x-ray diffraction and x-ray fluorescence techniques. The reaction products are quinoline derivatives, which are useful in the synthesis of carbohydrates and other organic compounds. Control experiments were performed to ensure that the reactivity of indium trifluoromethanesulfonate was not due to contaminants or impurities. A more efficient method for synthesizing indium trifluoromethanesulfonate was developed in order to avoid the use of toxic solvents like diphenyl ether. This process involves amines as nucleophiles, which are activated by transfer reactions with carbon tetrFormel:C3F9InO9S3Reinheit:Min. 95%Farbe und Form:SolidMolekulargewicht:562.03 g/molIndium trifluoromethanesulfonate
CAS:Formel:C3F9InO9S3Reinheit:95%Farbe und Form:Solid, Chunks or Crystalline PowderMolekulargewicht:562.01Indium(III) Trifluoromethanesulfonate
CAS:Kontrolliertes ProduktStability Hygroscopic, Moisture Sensitive
Applications Indium(III) trifluoromethanesulfonate is a catalyst that is used for hetero Diels-Alder reactions including intermolecular Diels-Alder reactions. It is also a catalyst for efficient acylation of alcohols, phenols and amines.
References Kamlesh, K.C., et al.: Synlett, 1999, 1743 (1999), Ali, T., et al.: Tetrahedron Lett., 40, 5621 (1999)Formel:C3F9InO9S3Farbe und Form:WhiteMolekulargewicht:562.03Methanesulfonic acid, 1,1,1-trifluoro-, indium(3+) salt (3:1)
CAS:Formel:CHF3InO3SReinheit:98%Farbe und Form:SolidMolekulargewicht:264.8950496







