379387
二硫代乙二酰胺
97%
别名:
乙二硫二胺, 二硫代草酰胺
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关于此项目
线性分子式:
NH2CSCSNH2
化学文摘社编号:
分子量:
120.20
MDL number:
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-203-9
Beilstein/REAXYS Number:
605577
Assay:
97%
Form:
powder
Quality Level
assay
97%
form
powder
mp
≥300 °C (lit.)
solubility
ethanol: soluble 40 mg/10 mL, clear, red
functional group
amine
SMILES string
NC(=S)C(N)=S
InChI
1S/C2H4N2S2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
InChI key
OAEGRYMCJYIXQT-UHFFFAOYSA-N
General description
据报道，二硫代草酰胺与 Ni (II) 形成复合物。
Application
二硫代酰胺可用于以下研究：
- 溶剂热条件下噻唑并噻唑连接的多孔有机聚合物的合成。
- 以槲皮素为改性剂制备修饰玻碳电极，研究其重要的黄酮类化合物衍生物槲皮素的电化学属性。
- 用于银离子分离和浓缩的新型二硫代恶胺-甲醛螯合树脂的合成。
- N,N′ 的合成-二取代二硫代酰胺。
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Nickel (II) complexes with dithiooxamide, N, N'-di-methyl-and N, N'-di-hydroxyethyl-dithiooxamide.
Peyronel G, et al.
Inorgorganica Chimica Acta, 5, 627-633 (1971)
Preparation of Dithiooxamide Derivatives.
Hurd RN, et al.
The Journal of Organic Chemistry, 26(10), 3980-3987 (1961)
Xiang Zhu et al.
Chemical communications (Cambridge, England), 50(95), 15055-15058 (2014-10-21)
Thiazolothiazole-linked porous organic polymers have been synthesized from a facile catalyst-free condensation reaction between aldehydes and dithiooxamide under solvothermal conditions. The resultant porous frameworks exhibit a highly selective uptake of CO2 over N2 under ambient conditions.
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 379387-25G | 04061831837056 |
| 379387-5G | 04061831837063 |