CAS 128008-30-0
:indium trifluoromethanesulphonate
Description:
Indium trifluoromethanesulphonate, with the CAS number 128008-30-0, is an inorganic compound characterized by its indium center coordinated with trifluoromethanesulfonate (triflate) ligands. This compound typically appears as a white to off-white solid and is known for its solubility in polar organic solvents, making it useful in various chemical applications. Indium trifluoromethanesulphonate is often employed as a Lewis acid catalyst in organic synthesis, particularly in reactions involving electrophilic aromatic substitutions and other transformations where activation of substrates is required. Its strong electron-withdrawing triflate groups enhance its reactivity, allowing it to facilitate reactions under mild conditions. Additionally, this compound is of interest in materials science and nanotechnology, particularly in the development of indium-based materials and thin films. Safety precautions should be observed when handling this compound, as it may pose health risks if inhaled or ingested, and appropriate protective equipment should be used.
Formula:C3F9InO9S3
InChI:InChI=1/3CHF3O3S.In/c3*2-1(3,4)8(5,6)7;/h3*(H,5,6,7);/q;;;+3/p-3
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]
Synonyms:- 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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Found 8 products.
Indium(III) trifluoromethanesulfonate, 99% min
CAS:<p>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</p>Formula:C3F9InO9S3Purity:99%Molecular weight:562.01Indium(III) trifluoromethanesulfonate, 99% (Indium triflate)
CAS:<p>Indium(III) trifluoromethanesulfonate, 99% (Indium triflate)</p>Formula:In(CF3SO3)3Purity:99%Color and Shape:white pwdr.Molecular weight:562.02Indium(lll) trifluoromethanesulfonate
CAS:Formula:In(CF3SO3)3Purity:≥ 99.0%Color and Shape:White to off-white crystalline powder or crystalsMolecular weight:562.02Indium trifluoromethanesulphonate
CAS:<p>Indium trifluoromethanesulphonate</p>Purity:95%Color and Shape:PowderMolecular weight:562.03g/molIndium(III) trifluoromethanesulfonate
CAS:<p>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 tetr</p>Formula:C3F9InO9S3Purity:Min. 95%Color and Shape:SolidMolecular weight:562.03 g/molIndium trifluoromethanesulfonate
CAS:Formula:C3F9InO9S3Purity:95%Color and Shape:Solid, Chunks or Crystalline PowderMolecular weight:562.01Indium(III) Trifluoromethanesulfonate
CAS:Controlled Product<p>Stability Hygroscopic, Moisture Sensitive<br>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.<br>References Kamlesh, K.C., et al.: Synlett, 1999, 1743 (1999), Ali, T., et al.: Tetrahedron Lett., 40, 5621 (1999)<br></p>Formula:C3F9InO9S3Color and Shape:WhiteMolecular weight:562.03Methanesulfonic acid, 1,1,1-trifluoro-, indium(3+) salt (3:1)
CAS:Formula:CHF3InO3SPurity:98%Color and Shape:SolidMolecular weight:264.8950496







