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About This Item
线性分子式:
CH3CH2SNa
CAS号:
分子量:
84.12
Beilstein:
3593647
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
推荐产品
等級
technical grade
化驗
80%
SMILES 字串
CCS[Na]
InChI
1S/C2H6S.Na/c1-2-3;/h3H,2H2,1H3;/q;+1/p-1
InChI 密鑰
QJDUDPQVDAASMV-UHFFFAOYSA-M
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一般說明
本文研究了 FeCl 2 或 FeCl 3 与乙硫代硫酸钠在 N -甲基甲酰胺 (NMF) 中的反应。研究了乙硫代硫酸钠与取代 1，2-二硫戊环-3-硫酮的反应。
應用
乙硫代硫酸钠可用于 G-25 凝胶过滤 (ox)-状态 FeMo 辅因子 \ [FeMoco (ox)]（来自 棕色固氮菌 固氮酶）的 N -甲基甲酰胺的平衡滴定。它可用于合成一系列混合化合物，这些化合物结合了维生素 E 的药效氧化还原部分和负责 I 类抗心律失常药普鲁卡因胺和利多卡因的抗心律失常特性的关键特征。
訊號詞
Danger
危險聲明
危險分類
Skin Corr. 1B
安全危害
儲存類別代碼
8A - Combustible corrosive hazardous materials
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
其他客户在看
Reactivity of substituted 1, 2-dithiole-3-thiones with sodium ethanethiolate: a convenient route to a novel heterocycle.
Largeron M, et al.
Tetrahedron, 43(15), 3421-3428 (1987)
Patrick Frank et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 10(4), 373-382 (2005-05-03)
The reaction of FeCl(2) or FeCl(3) with sodium ethanethiolate (SEt) in N-methylformamide (NMF) has been reevaluated to rectify a previous Fe(II) oxidation artifact. On titrating Fe(II) with EtS(-) concentrations up to 12 mol Eq, new features in the UV/vis spectrum
P Frank et al.
Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 6(7), 683-697 (2001-10-30)
Equilibrium titrations in N-methylformamide (NMF) of G-25 gel filtered (ox)-state FeMo cofactor [FeMoco(ox)] from Azotobacter vinelandii nitrogenase were carried out using sodium ethanethiolate and followed using UV/Vis absorption spectroscopy. For Fe-Moco(ox), a non-linear least squares (NLLSQ) fit to the data
Maria Koufaki et al.
Bioorganic & medicinal chemistry, 11(23), 5209-5219 (2003-11-08)
We have synthesized a series of hybrid compounds combining the pharmacophoric redox moieties of vitamin E and key features responsible for the antiarrhythmic properties of the class I antiarrhythmics procainamide and lidocaine. Procainamide analogue (2a) and lidocaine analogues (14a) and
Pinar Kasaplar et al.
Bioorganic chemistry, 38(5), 186-189 (2010-07-27)
The mechanism of action for alpha,beta-unsaturated lactones can be explained by their Michael acceptor properties. They have the potential of being covalently binding inhibitors by accepting nucleophiles from target proteins. In this work, Michael addition reactions of ethanethiol with 6-bicycloaryl
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