CAS 59163-91-6
:Methanesulfonic acid, 1,1,1-trifluoro-, iron(2+) salt (2:1)
Description:
Methanesulfonic acid, 1,1,1-trifluoro-, iron(2+) salt (2:1) is a coordination compound characterized by its iron(II) salt form with methanesulfonic acid and trifluoromethyl groups. This compound typically exhibits properties associated with both the iron(II) ion and the sulfonic acid moiety, including solubility in polar solvents and potential catalytic activity. The presence of trifluoromethyl groups can enhance the compound's stability and influence its reactivity, making it useful in various chemical applications. Iron(II) salts are known for their ability to participate in redox reactions, and the methanesulfonic acid component contributes to the compound's acidity and potential as a proton donor. The 2:1 stoichiometry indicates that two methanesulfonic acid molecules coordinate with one iron(II) ion, which may affect the compound's overall stability and solubility. This substance is of interest in fields such as catalysis, materials science, and potentially in pharmaceuticals, owing to its unique chemical properties and structural characteristics.
Formula:CHF3O3SFe
InChI:InChI=1S/CHF3O3S.Fe/c2-1(3,4)8(5,6)7;/h(H,5,6,7);
InChI key:InChIKey=QZLVALRWETVYSE-UHFFFAOYSA-N
SMILES:C(S(=O)(=O)O)(F)(F)F.[Fe]
Synonyms:- Ferrous triflate
- Iron bis(trifluoromethanesulfonate)
- Iron ditriflate
- Iron(2+) Bis(Trifluoromethanesulfonate)
- Iron(2+) triflate
- Iron(2+) trifluoromethanesulfonate
- Iron(II) triflate
- Methanesulfonic acid, 1,1,1-trifluoro-, iron(2+) salt (2:1)
- Methanesulfonic acid, trifluoro-, iron(2+) salt
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Found 7 products.
Iron(II) trifluoromethanesulfonate, 98% (Iron triflate)
CAS:<p>Iron(II) trifluoromethanesulfonate, 98% (Iron triflate)</p>Formula:Fe(CF3SO3)2Purity:98%Color and Shape:off-white to brown pwdr.Molecular weight:353.99IRON(II) TRIFLUOROMETHANESULFONATE
CAS:Formula:C2F6FeO6S2Purity:98%Color and Shape:SolidMolecular weight:353.9832Iron (II) Trifluoromethanesulfonate
CAS:Iron (II) TrifluoromethanesulfonateFormula:·2CF3O3S·FePurity:97%Color and Shape: white to grey to purple. brown crystals or powderMolecular weight:353.98g/molIron(II) trifluoromethanesulfonate
CAS:<p>Iron(II) trifluoromethanesulfonate is a catalyst that can be used as an efficient method for organic synthesis. It has been shown to be effective in the reaction mechanism of hydrogenation, epoxidation, and carbonylation reactions. The catalyst is also useful in pharmaceutical preparations such as the synthesis of β-lactam antibiotics and synthetic process reactions such as conversion of nitrobenzene to nitroethane, chlorobenzene to dichlorobenzenes, and ethylbenzene to styrene. Iron(II) trifluoromethanesulfonate reacts with sulfoxides or sulfones to form a mixture of oximes, thioximes, or oxazetidines. The x-ray absorption spectra show that iron(II) trifluoromethanesulfonate binds nitrogen atoms through hydrogen bonding interactions. The nmr spectra also confirm this structure. Iron(II)</p>Formula:C2F6FeO6S2Purity:Min. 95%Color and Shape:PowderMolecular weight:353.99 g/molIron(II) trifluoromethanesulfonate
CAS:Formula:C2F6FeO6S2Purity:95%Color and Shape:SolidMolecular weight:353.97Iron(II) Trifluoromethanesulfonate
CAS:Controlled Product<p>Applications Iron(II) Trifluoromethanesulfonate acts as a catalyst for hydrosilylation and hydroboration of alkenes and alkynes to give silane and borane adducts. Reagent in the preparation of organometallic inhibitors of UFM1-activating enzymes UBAS.<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Challinor, A. J., et al.: Adv. Synth. Catal., 358, 2404 (2016); Da Silva, S. R., et al.: Biorg. Med. Chem. Lett., 26, 4542 (2016)<br></p>Formula:C2F6FeO6S2Color and Shape:Off-White To Light RedMolecular weight:353.98
