| Weight | 133.197 g/mol |
|---|---|
| Formula | C3H3NOS2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
RHODANINE (141-84-4)
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#4099 in Chemistry
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- Solution Processable RhodanineBased Small Molecule Organic Photovoltaic Cells with a Power Conversion Efficiency of 6.1% (Advanced Energy Materials, 2012)
- Rhodanine azosulpha drugs as corrosion inhibitors for corrosion of 304 stainless steel in hydrochloric acid solution (Corrosion Science, 2002)
- A Rhodanine Flanked Nonfullerene Acceptor for Solution-Processed Organic Photovoltaics (Journal of the American Chemical Society, 2015)
- Determination of gallotannin with rhodanine (Analytical Biochemistry, 1988)
- Rhodanine as a Privileged Scaffold in Drug Discovery (Current Medicinal Chemistry, 2009)
- Synthesis and in vivo antidiabetic activity of novel dispiropyrrolidines through [3+2] cycloaddition reactions with thiazolidinedione and rhodanine derivatives. (European Journal of Medicinal Chemistry, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(=O)NC(=S)S1
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InChIKeyKIWUVOGUEXMXSV-UHFFFAOYSA-N
- Pubchem - RHODANINE
- Wikipedia - rhodanine
Rhodanine is a 5-membered heterocyclic organic compound possessing a thiazolidine core. It was first discovered in 1877 by Marceli Nencki who named it "Rhodaninsaure" in reference to its synthesis from ammonium rhodanide (known as ammonium thiocyanate to modern chemists) and chloroacetic acid in water. Rhodanines can also be prepared by the reaction of carbon disulfide, ammonia, and chloroacetic acid, which proceeds via an intermediate dithiocarbamate.
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(5E)-5-(3-hydroxy-4-methoxybenzylidene)-3-methyl-2-thioxo-1,3-thiazolidin-4-one
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22656-77-5
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RHODANINE
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