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化驗
97%
形狀
liquid
折射率
n20/D 1.376 (lit.)
bp
90.5 °C (lit.)
密度
1.234 g/mL at 25 °C (lit.)
SMILES 字串
CCSC(=O)C(F)(F)F
InChI
1S/C4H5F3OS/c1-2-9-3(8)4(5,6)7/h2H2,1H3
InChI 密鑰
VGGUKFAVHPGNBF-UHFFFAOYSA-N
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應用
S-Ethyl trifluorothioacetate was used to selectively trifluoroacetylate amino groups in proteins.
訊號詞
Danger
危險聲明
危險分類
Flam. Liq. 2
儲存類別代碼
3 - Flammable liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
68.0 °F - closed cup
閃點（°C）
20 °C - closed cup
個人防護裝備
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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
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
M Kamo et al.
European journal of biochemistry, 255(1), 162-171 (1998-08-06)
A vapor of S-ethyltrifluorothioacetate was found to specifically cleave the amino side of serine and threonine peptide bonds. The cleavage reactions were carried out at 50 degrees C for 6 h-24 h or at 30 degrees C for 24 h.
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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