CAS 3988-99-6
:2-(2-thienylthio)thiophene
Description:
2-(2-Thienylthio)thiophene is an organic compound characterized by its unique structure, which includes a thiophene ring and a thienylthio substituent. This compound features a five-membered aromatic ring containing sulfur atoms, contributing to its distinct electronic properties. The presence of the thienylthio group enhances its potential for applications in organic electronics, particularly in organic semiconductors and photovoltaic devices, due to its ability to facilitate charge transport. Additionally, the compound exhibits interesting optical properties, making it suitable for use in light-emitting devices. Its solubility and stability can vary depending on the solvent and environmental conditions, which are important factors to consider in practical applications. The compound's reactivity may also be influenced by the presence of sulfur atoms, which can participate in various chemical reactions, including nucleophilic substitutions. Overall, 2-(2-thienylthio)thiophene is a notable compound in the field of materials science and organic chemistry, with potential implications in advanced electronic materials.
Formula:C8H6S3
InChI:InChI=1/C8H6S3/c1-3-7(9-5-1)11-8-4-2-6-10-8/h1-6H
SMILES:c1cc(sc1)Sc1cccs1
Synonyms:- Thiophene, 2,2'-thiobis-
- 2,2'-Sulfanediyldithiophene
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
Di-2-thienyl sulfide, 97%
CAS:<p>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 Sci</p>Formula:C8H6S3Purity:97%Color and Shape:Clear colorless to yellow to brown, LiquidMolecular weight:198.32Dithienyl sulphide
CAS:<p>Dithienyl sulphide is a heterocyclic compound that contains a morpholine ring and two nitro groups. It has been reported to be an acceptor for furyl, piperidine, and wittig reactions. The kinetic data of the reactions have been determined by inorganic acid and inorganic bases. This chemical is also used as a sulfide marker for analytical methods, such as gas chromatography-mass spectrometry (GC-MS). Dithienyl sulphide has functional groups including sulfide, allyl, and disulphides.</p>Formula:C8H6S3Purity:Min. 95%Molecular weight:198.33 g/mol



