Molecule:100618
From ChemWiki
molecule
| Properties | |
|---|---|
| CID | 6409 |
| CAS | 75-89-8 |
| IUPAC-Name | 2,2,2-tris(fluoranyl)ethanol |
| Abbreviation | TFE |
| Trivialname | 2,2,2-TRIFLUOROETHANOL |
| Exact mass | 100.01359920 |
| Molecular formula | C2H3F3O |
| LogP | 0.4 |
| Has vendors | true |
| Molecular role | n/a |
| Synonyms | 2,2,2-TRIFLUOROETHANOL, Trifluoroethanol, Ethanol, 2,2,2-trifluoro-, trifluoro ethanol, 2,2,2-Trifluoroethyl alcohol, Trifluoroethyl alcohol, 2,2,2-Trifluoroethan-1-Ol, Fluorinol 85, tfetoh, TFE, Perfluoro-1,1-dihydroethanol, CF3CH2OH, NSC 451, 2,2,2-trifluoro-ethanol, beta,beta,beta-Trifluoroethyl alcohol, MFCD00004672, 8T8I76KYF1, CHEBI:42330, NSC-451, .beta.,.beta.,.beta.-Trifluoroethyl alcohol, ETF, 2,2,2-TRIFLUORETHANOL, 1h,1h-trifluoroethanol, EINECS 200-913-6, BRN 1733203, ethanol, 2,2,2-trifluoro, trifluorethanol, trifluroethanol, UNII-8T8I76KYF1, AI3-25486, trifluoroethylalcohol, BETA,BETA,BETA-TRIFLUOROETHANOL, 2,2-Trifluoroethanol, 2,2,-trifluoroethanol, 2,2,2trifluoroethanol, 2,2,2-trifluoroetanol, 2,2,2-trifluoroethoxy, 2,2,2-trifluroethanol, 2 2 2-trifluoroethanol, 2,2,2 trifluoroethanol, 2.2,2-trifluoroethanol, 2.2.2-trifluoroethanol, 2,2,2-trifluoroethanole, WLN: Q1XFFF, 2,2,2-trifloro ethanol, DSSTox_CID_1751, 2,2,2 trifluoro-ethanol, 2,2,2,-trifluoroethanol, 2,2,2-tri-fluoroethanol, 2,2,2-trifluoro ethanol, Trifluoroethanol (Related), EC 200-913-6, 2,2-Trifluoroethyl alcohol, SCHEMBL4869, 2,2,2-trifluoro -ethanol, DSSTox_RID_76304, 2,2,2-trifluoroethylalcohol, DSSTox_GSID_21751, [[Synonym::TRIFLUOROETHANOL [MI]]], 4-01-00-01370 (Beilstein Handbook Reference), 1,1,1-Trifluoro-2-ethanol, CHEMBL116675, NSC451, DTXSID0021751, Trifluoroethyl alcohol (Related), beta, beta, beta-trifluoroethanol, ETHANOL,2,2,2-TRIFLUORO, ACT10236, BCP31089, ZINC3860799, Tox21_200905, 2,2,2-Trifluoroethanol, NMR grade, BBL008539, STK260853, .beta.,.beta.-Trifluoroethyl alcohol, AKOS000119834, DB03226, CAS-75-89-8, NCGC00248871-01, NCGC00258459-01, BP-21406, VS-01941, AM20100728, T0435, C93508, 2,2,2-Trifluoroethanol, ReagentPlus(R), >=99%, 2,2,2-Trifluoroethanol redistilled from glass grade, J-506750, Q2474643, F0001-1907, 2,2,2-Trifluoroethanol, analytical standard, for NMR spectroscopy, Trifluoroethanol;Ethanol, 2,2,2-trifluoro-;Trifluoroethyl alcohol, 2,2,2-Trifluoroethanol, BioUltra, for molecular biology, >=99.0% (GC) |
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Molecule is used on following pages
publication
- Phenoxazine-Sensitized CO2-to-CO Reduction with an Iron Porphyrin Catalyst: A Redox Properties-Catalytic Performance Study
- Visible-Light-Driven Conversion of CO2 to CH4 with an Organic Sensitizer and an Iron Porphyrin Catalyst
- Toward Visible-Light Photochemical CO2‑to-CH4 Conversion in Aqueous Solutions Using Sensitized Molecular Catalysis
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction
investigation
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results obtained with Co2+ catalyst
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/results CO2+ experiments
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/CO2+ results from SI
- Exchange Coupling Determines Metal-Dependent Efficiency for Iron- and Cobalt-Catalyzed Photochemical CO2 Reduction/Results Co2+ experiments taken from SI
Molecule roles
| Investigation type | Hydrogen donor |
|---|---|
| Photocatalytic CO2 conversion experiments |
|
| Cyclic Voltammetry experiments |  |
