Molecule:100618: Difference between revisions
From ChemWiki
molecule
(auto-generated) |
No edit summary |
||
(10 intermediate revisions by 3 users not shown) | |||
Line 1: | Line 1: | ||
{{Molecule | {{Molecule | ||
|abbrev=TFE | |||
|trivialname=2,2,2-trifluoroethanol | |||
|cid=6409 | |cid=6409 | ||
|iupacName=2,2,2-tris(fluoranyl)ethanol | |iupacName=2,2,2-tris(fluoranyl)ethanol | ||
Line 5: | Line 7: | ||
|molecularFormula=C<sub>2</sub>H<sub>3</sub>F<sub>3</sub>O | |molecularFormula=C<sub>2</sub>H<sub>3</sub>F<sub>3</sub>O | ||
|logP=0.4 | |logP=0.4 | ||
|synonyms= | |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 | ||
|cas=75-89-8 | |cas=75-89-8 | ||
|hasVendors=true | |hasVendors=true | ||
|moleculeKey=RHQDFWAXVIIEBN-UHFFFAOYSA-N | |moleculeKey=RHQDFWAXVIIEBN-UHFFFAOYSA-N | ||
|molOrRxn= | |molOrRxn=-INDIGO-12132211472D | ||
0 0 0 0 0 0 0 0 0 0 0 V3000 | 0 0 0 0 0 0 0 0 0 0 0 V3000 | ||
Line 34: | Line 33: | ||
M V30 END CTAB | M V30 END CTAB | ||
M END | M END | ||
|smiles=C(C(F)(F)F)O | |smiles=C(C(F)(F)F)O | ||
|inchi=1S/C2H3F3O/c3-2(4,5)1-6/h6H,1H2 | |inchi=1S/C2H3F3O/c3-2(4,5)1-6/h6H,1H2 | ||
|inchikey=RHQDFWAXVIIEBN-UHFFFAOYSA-N | |inchikey=RHQDFWAXVIIEBN-UHFFFAOYSA-N | ||
|width= | |width=75px | ||
|height= | |height=50px | ||
|float=none | |float=none | ||
}} | }} |
Latest revision as of 11:25, 22 May 2024
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 |
Click here to copy MOL-file.
Click here to show SMILES and InChI.
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