Rhodanine, 98+%, Thermo Scientific Chemicals
Rhodanine, 98+%, Thermo Scientific Chemicals
Rhodanine, 98+%, Thermo Scientific Chemicals
Rhodanine, 98+%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

Rhodanine, 98+%, Thermo Scientific Chemicals

CAS: 141-84-4 | C3H3NOS2 | 133.183 g/mol
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Catalog NumberQuantity
ALFA18293.1425 g
Catalog number ALFA18293.14
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Quantity:
25 g
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Chemical Identifiers
CAS2206-27-1
IUPAC Name(²H₃)methanesulfinyl(²H₃)methane
Molecular FormulaC2H6OS
InChI KeyIAZDPXIOMUYVGZ-WFGJKAKNSA-N
SMILES[2H]C([2H])([2H])S(=O)C([2H])([2H])[2H]
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SpecificationsSpecification SheetSpecification Sheet
D-Enrichment>=99.0 %
Appearance (Form)Liquid
Water=<0.1 % (Coulometric)
Appearance (Color)Clear colorless
Rhodanine inhibits the multiplication of echovirus 12 and the development of virus-induced morphologic changes. It has been used in tannase assay in cultures of tannin degrading fungi. It possess anticonvulsant, antibacterial, antiviral and antidiabetic activities.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Rhodanine inhibits the multiplication of echovirus 12 and the development of virus-induced morphologic changes. It has been used in tannase assay in cultures of tannin degrading fungi. It possess anticonvulsant, antibacterial, antiviral and antidiabetic activities.

Solubility
Soluble in water (2.25 g/L at 20°C).

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. H.J.Eggers; M.A.Koch; A.Furst; G.D.Daves; J.J.Wilczynski; K.Folkers. Rhodanine: a selective inhibitor of the multiplication of echovirus 12. Science. 1970, 167,(3916), 294-297.
  2. W.T.Sing; C.L.Lee; S.L.Yeo; S.P.Lim; M.M.Sim. Arylalkylidene rhodanine with bulky and hydrophobic functional group as selective HCV NS3 protease inhibitor. Bioorganic & Medicinal Chemistry Letters. 2001, 11,(2), 91-94.
  3. Reagent for Ag and Au.