CAS 128008-30-0
:trifluorometanossulfonato de índio
- 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)
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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
Fórmula:C3F9InO9S3Pureza:99%Peso molecular:562.01Indium(III) trifluoromethanesulfonate, 99% (Indium triflate)
CAS:Indium(III) trifluoromethanesulfonate, 99% (Indium triflate)
Fórmula:In(CF3SO3)3Pureza:99%Cor e Forma:white pwdr.Peso molecular:562.02Indium(lll) trifluoromethanesulfonate
CAS:Fórmula:In(CF3SO3)3Pureza:≥ 99.0%Cor e Forma:White to off-white crystalline powder or crystalsPeso molecular:562.02Indium trifluoromethanesulphonate
CAS:Indium trifluoromethanesulphonatePureza:95%Cor e Forma:PowderPeso molecular: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 tetrFórmula:C3F9InO9S3Pureza:Min. 95%Cor e Forma:SolidPeso molecular:562.03 g/molIndium trifluoromethanesulfonate
CAS:Fórmula:C3F9InO9S3Pureza:95%Cor e Forma:Solid, Chunks or Crystalline PowderPeso molecular:562.01Indium(III) Trifluoromethanesulfonate
CAS:Produto ControladoStability 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)Fórmula:C3F9InO9S3Cor e Forma:WhitePeso molecular:562.03Methanesulfonic acid, 1,1,1-trifluoro-, indium(3+) salt (3:1)
CAS:Fórmula:CHF3InO3SPureza:98%Cor e Forma:SolidPeso molecular:264.8950496







