379387
Dithiooxamide
97%
Sinônimo(s):
Dithiooxalic diamide, Rubeanic acid
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About This Item
Fórmula linear:
NH2CSCSNH2
Número CAS:
Peso molecular:
120.20
Beilstein:
605577
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Nível de qualidade
Ensaio
97%
forma
powder
pf
≥300 °C (lit.)
solubilidade
ethanol: soluble 40 mg/10 mL, clear, red
grupo funcional
amine
cadeia de caracteres SMILES
NC(=S)C(N)=S
InChI
1S/C2H4N2S2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
chave InChI
OAEGRYMCJYIXQT-UHFFFAOYSA-N
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Descrição geral
Dithiooxamide is reported to form complexes with Ni(II).
Aplicação
Dithiooxamide may be used in the following studies:
- Synthesis of thiazolothiazole-linked porous organic polymers under solvothermal conditions.
- As modifier to prepare the modified glassy carbon electrode, used to investigate the electrochemical properties of quercetin, an important flavonoid derivative.
- Synthesis of new chelating resin of dithiooxamide (rubeanic acid)-formaldehyde (DTOF), used in separation and concentration of silver ions.
- Synthesis of N,N′-disubstituted dithiooxamides.
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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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.
Preparation of Dithiooxamide Derivatives.
Hurd RN, et al.
The Journal of Organic Chemistry, 26(10), 3980-3987 (1961)
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)
Ayşen Demir Mülazımoğlu et al.
Sensors (Basel, Switzerland), 12(4), 3916-3928 (2012-06-06)
Electrochemical oxidation of quercetin, as an important biological molecule, has been studied in non-aqueous media using cyclic voltammetry, electrochemical impedance spectroscopy and scanning electron microscopy. To investigate the electrochemical properties of quercetin, an important flavonoid derivative, on a different surface
Zeliyha Celik et al.
Journal of hazardous materials, 174(1-3), 556-562 (2009-10-13)
In this study, a new chelating resin of dithiooxamide (rubeanic acid)-formaldehyde (DTOF) has been synthesized by the reaction of dithiooxamide and formaldehyde. Also a well-known chelating resin of thiourea (thiooxamide)-formaldehyde (TUF) has been prepared by the reaction of thiourea and
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