Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H5FO |
| Molecular Weight | 64.0589 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OCCF
InChI
InChIKey=GGDYAKVUZMZKRV-UHFFFAOYSA-N
InChI=1S/C2H5FO/c3-1-2-4/h4H,1-2H2
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Preclinical evaluation of an 18F-labelled beta1-adrenoceptor selective radioligand based on ICI 89,406. | 2010-05 |
|
| Influence of fluorine atoms and aromatic rings on the acidity of ethanol. | 2009-10-08 |
|
| Molecular self-recognition: rotational spectra of the dimeric 2-fluoroethanol conformers. | 2009 |
|
| Phenolic derivatives from soy flour ethanol extract are potent in vitro quinone reductase (QR) inducing agents. | 2008-11-26 |
|
| Synthesis and biological evaluation of substituted [18F]imidazo[1,2-a]pyridines and [18F]pyrazolo[1,5-a]pyrimidines for the study of the peripheral benzodiazepine receptor using positron emission tomography. | 2008-07-10 |
|
| Tailoring the key in a molecular lock-and-key model system: the propylene oxide...2-fluoroethanol complex. | 2008-05-07 |
|
| Metabolism of mono- and dihalogenated C1 and C2 compounds by Xanthobacter autotrophicus growing on 1,2-dichloroethane. | 2007-04 |
|
| Energetics of C-F, C-Cl, C-Br, and C-I bonds in 2-haloethanols. enthalpies of formation of XCH(2)CH(2)OH (X = F, Cl, Br, I) compounds and of the 2-hydroxyethyl radical. | 2007-03-08 |
|
| The observation of a large gauche preference when 2-fluoroethylamine and 2-fluoroethanol become protonated. | 2004-03-07 |
|
| Kinetics and mechanism of the proton transfer to CpFe(dppe)H: absence of a direct protonation at the metal site. | 2003-09-10 |
|
| An automatic method to generate force-field parameters for hetero-compounds. | 2003-02 |
|
| Ethenesulfonamide and ethanesulfonamide derivatives, a novel class of orally active endothelin-A receptor antagonists. | 2001-11 |
|
| Ethenesulfonamide derivatives, a novel class of orally active endothelin-A receptor antagonists. | 2001-05 |
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| Code System | Code | Type | Description | ||
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6389
Created by
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158283
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DTXSID0059902
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9737
Created by
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Ethylene fluorohydrin
Created by
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206-740-2
Created by
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4M427A5HML
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371-62-0
Created by
admin on Mon Mar 31 22:23:19 GMT 2025 , Edited by admin on Mon Mar 31 22:23:19 GMT 2025
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SUBSTANCE RECORD
