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Sigma-Aldrich

S-Ethyl trifluorothioacetate

97%

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About This Item

Fórmula linear:
CF3COSC2H5
Número CAS:
Peso molecular:
158.14
Beilstein:
1761564
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

97%

Formulário

liquid

índice de refração

n20/D 1.376 (lit.)

p.e.

90.5 °C (lit.)

densidade

1.234 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCSC(=O)C(F)(F)F

InChI

1S/C4H5F3OS/c1-2-9-3(8)4(5,6)7/h2H2,1H3

chave InChI

VGGUKFAVHPGNBF-UHFFFAOYSA-N

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Aplicação

S-Ethyl trifluorothioacetate was used to selectively trifluoroacetylate amino groups in proteins[1].

Pictogramas

Flame

Palavra indicadora

Danger

Frases de perigo

Declarações de precaução

Classificações de perigo

Flam. Liq. 2

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

68.0 °F - closed cup

Ponto de fulgor (°C)

20 °C - closed cup

Equipamento de proteção individual

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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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
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
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.
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

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