CAS 534-25-8
:1,2-dithiole-3-thione
Description:
1,2-Dithiole-3-thione, also known as 1,2-dithiol-3-thione, is a heterocyclic compound characterized by a five-membered ring containing two sulfur atoms and one carbonyl group. Its molecular structure features a dithiole framework, which contributes to its unique chemical properties. This compound is typically a yellow to orange solid and is known for its role in various chemical reactions, particularly in the field of organic synthesis and as a potential precursor in the formation of other sulfur-containing compounds. 1,2-Dithiole-3-thione exhibits notable reactivity due to the presence of the thioketone functional group, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, it has been studied for its biological activities, including potential antioxidant properties. The compound is soluble in organic solvents, and its stability can be influenced by environmental factors such as temperature and light. Overall, 1,2-dithiole-3-thione is an important compound in both synthetic and applied chemistry.
Formula:C3H2S3
InChI:InChI=1/C3H2S3/c4-3-1-2-5-6-3/h1-2H
InChI key:InChIKey=LZENMJMJWQSSNJ-UHFFFAOYSA-N
SMILES:S=C1C=CSS1
Synonyms:- 1,2-Dithiol-3-thione
- 3H-1,2-dithiole-3-thione
- Broad ID:BRD-K91781484
- 1,2-Dithiole-3-thione
- 1,2-Dithiole-3-thione
- dithiole-3-thione
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Found 3 products.
3H-1,2-Dithiole-3-thione
CAS:Controlled ProductStability Stench
Applications A chemoprotective chemical. It is known to induce detoxication enzymes and inhibit chemica-induced tumors in multiple tissues.
References Otieno, M..A., et al.: Free Radical Biol. Med., 28, 944 (2000), Munday, R., et al.: Carcinogenesis, 25, 1721 (2004)Formula:C3H2S3Color and Shape:NeatMolecular weight:134.24
