CAS 1457-47-2
:3-Allylrhodanine
Description:
3-Allylrhodanine, with the CAS number 1457-47-2, is a chemical compound that belongs to the rhodanine family, characterized by its five-membered ring structure containing sulfur and nitrogen. This compound typically exhibits a yellow to orange color and is known for its potential biological activities, including antimicrobial and anti-inflammatory properties. The presence of the allyl group contributes to its reactivity, allowing for various chemical modifications and applications in organic synthesis. 3-Allylrhodanine can participate in nucleophilic reactions due to the electron-withdrawing nature of the rhodanine moiety, making it a valuable intermediate in the development of pharmaceuticals and agrochemicals. Additionally, its solubility in organic solvents and moderate stability under standard conditions make it suitable for laboratory use. However, as with many chemical substances, proper handling and safety precautions are essential due to potential toxicity and environmental impact. Overall, 3-Allylrhodanine is a compound of interest in both synthetic chemistry and medicinal research.
Formula:C6H7NOS2
InChI:InChI=1S/C6H7NOS2/c1-2-3-7-5(8)4-10-6(7)9/h2H,1,3-4H2
InChI key:InChIKey=GYGUTBCTEJBRAN-UHFFFAOYSA-N
SMILES:C(C=C)N1C(=O)CSC1=S
Synonyms:- 3-(2-Propen-1-yl)-2-thioxo-4-thiazolidinone
- Rhodanine, 3-allyl-
- 3-Allyl-4-oxo-2-thioxothiazolidine
- 4-Thiazolidinone, 3-(2-propenyl)-2-thioxo-
- 4-Thiazolidinone, 3-(2-propen-1-yl)-2-thioxo-
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
4-Thiazolidinone, 3-(2-propen-1-yl)-2-thioxo-
CAS:Formula:C6H7NOS2Purity:98%Color and Shape:SolidMolecular weight:173.25593-Allylrhodanine
CAS:Formula:C6H7NOS2Purity:>98.0%(GC)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:173.253-Allylrhodanine
CAS:<p>3-Allylrhodanine is an anti-bacterial agent that has been shown to inhibit the growth of bacteria by interacting with transition metal ions. It is used in wastewater treatment to remove carbon disulfide and its condensation products. 3-Allylrhodanine reacts with aldehydes to form ethyl orthoformate and chloride, which are then converted into 2-bromo-3-nitrobenzoic acid. This compound is metabolized by nitroreductase and nitroreductase reductase, which produce hydrogen bond and thermodynamic effects, respectively. 3-Allylrhodanine also has hormone receptor binding activity that may lead to an increase in nitric oxide levels.</p>Formula:C6H7NOS2Purity:Min. 95%Molecular weight:173.26 g/mol





