160342
2-Fluoroethanol
95%
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About This Item
Linear Formula:
FCH2CH2OH
CAS Number:
Molecular Weight:
64.06
Beilstein:
1730857
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
vapor pressure
16 mmHg ( 20 °C)
Assay
95%
form
liquid
refractive index
n20/D 1.365 (lit.)
bp
103 °C/757 mmHg (lit.)
mp
−26.5 °C (lit.)
density
1.091 g/mL at 25 °C (lit.)
SMILES string
OCCF
InChI
1S/C2H5FO/c3-1-2-4/h4H,1-2H2
InChI key
GGDYAKVUZMZKRV-UHFFFAOYSA-N
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General description
The microwave spectra of two isotopic species of 2-fluoroethanol have been investigated. The Gg′ conformer of 2-fluoroethanol was isolated in low-temperature noble gas matrices. Single-photon IR photolysis of 2-fluoroethanol in solid argon has been investigated.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 1 Oral - Flam. Liq. 3
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
93.2 °F - closed cup
Flash Point(C)
34 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Site-selective infrared photoisomerizations of 2-fluoroethanol in low-temperature matrices
Pourcin J, et al.
Journal of Molecular Spectroscopy, 109(1) (1985)
Infrared laser photoisomerization of 2-fluoroethanol in argon.
Hoffman III WF and Shirk JS.
Chemical Physics, 78(3), 331-338 (1983)
Microwave Spectrum and Intramolecular Hydrogen Bonding in 2-Fluoroethanol.
Buckton KS and Azrak RG.
J. Chem. Phys. , 52(11), 5652-5655 (1970)
Kiel D Neumann et al.
Journal of labelled compounds & radiopharmaceuticals, 60(7), 337-342 (2017-04-14)
O-(2-Fluoroethyl)-O-(p-nitrophenyl) methylphosphonate 1 is an organophosphate cholinesterase inhibitor that creates a phosphonyl-serine covalent adduct at the enzyme active site blocking cholinesterase activity in vivo. The corresponding radiolabeled O-(2-[
Xunchen Liu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(1), 270-277 (2008-12-02)
Fluoroalcohols show competitive formation of intra- and intermolecular hydrogen bonds, a property that may be crucial for the protein-altering process in a fluoroalcohol/water solution. In this study, we examine the intra- and intermolecular interactions of 2-fluoroethanol (FE) in its dimeric
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