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S-Ethyltrifluorthioacetat
97%
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About This Item
Lineare Formel:
CF3COSC2H5
CAS-Nummer:
Molekulargewicht:
158.14
Beilstein:
1761564
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Assay
97%
Form
liquid
Brechungsindex
n20/D 1.376 (lit.)
bp
90.5 °C (lit.)
Dichte
1.234 g/mL at 25 °C (lit.)
SMILES String
CCSC(=O)C(F)(F)F
InChI
1S/C4H5F3OS/c1-2-9-3(8)4(5,6)7/h2H2,1H3
InChIKey
VGGUKFAVHPGNBF-UHFFFAOYSA-N
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Anwendung
S-Ethyl trifluorothioacetate was used to selectively trifluoroacetylate amino groups in proteins[1].
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Flam. Liq. 2
Lagerklassenschlüssel
3 - Flammable liquids
WGK
WGK 3
Flammpunkt (°F)
68.0 °F - closed cup
Flammpunkt (°C)
20 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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S Doonan et al.
The Italian journal of biochemistry, 28(6), 441-455 (1979-11-01)
Results obtained as part of a study of the primary structure of mitochondrial aspartate aminotransferase from pig heart are described. In particular, the S-aminoethylated protein was digested with trypsin and with the lysine specific protease from A. mellea. In the
V D Mehta et al.
Bioconjugate chemistry, 5(3), 257-261 (1994-05-01)
Fluorinated proteins have been synthesized and characterized as potential in vivo 19F magnetic resonance imaging (MRI) and spectroscopy (MRS) agents. Proteins labeled with fluorine include bovine serum albumin, gamma-globulin, and purified immunoglobulin (IgG). The amino groups in proteins were selectively
P Adriaensens et al.
European journal of biochemistry, 177(2), 383-394 (1988-11-01)
A 19F-labeled derivative of hen egg-white lysozyme, in which the six epsilon-amino groups are trifluoroacetylated (LF6), was prepared by reaction of lysozyme with S-ethyltrifluorothioacetate. The reaction mixture was fractionated by cation-exchange chromatography at pH 7.3. A comparison of the circular
María Eliana Defonsi Lestard et al.
The Journal of chemical physics, 131(21), 214303-214303 (2009-12-09)
The molecular structure and conformational properties of S-ethyl trifluorothioacetate, CF(3)COSCH(2)CH(3), were determined in the gas phase by electron diffraction and vibrational spectroscopy (IR and Raman). The experimental investigations were supplemented by ab initio (Moller Plesset of second order) and density
K L Hastings et al.
Immunopharmacology and immunotoxicology, 17(1), 201-213 (1995-02-01)
Halothane hepatitis appears to result from an inappropriate immune response to the products of halothane metabolism. Attempts to produce an animal model for halothane hepatitis have been largely unsuccessful. Although guinea pigs produce neoantigens following treatment with halothane, the subsequent
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