CAS 55968-16-6
:1H-Indole,2-(2-thienyl)-
Description:
1H-Indole, 2-(2-thienyl)-, with the CAS number 55968-16-6, is an organic compound characterized by its fused bicyclic structure, which consists of an indole moiety and a thiophene ring. The indole part is a five-membered ring containing nitrogen, while the thiophene is a five-membered ring containing sulfur. This compound exhibits properties typical of heterocyclic aromatic compounds, including potential biological activity and the ability to participate in various chemical reactions due to the presence of the nitrogen and sulfur atoms. It is often studied for its applications in pharmaceuticals, agrochemicals, and materials science due to its unique electronic properties and ability to form π-stacking interactions. The presence of the thiophene ring can enhance the compound's solubility and reactivity, making it of interest in organic synthesis and medicinal chemistry. Additionally, compounds like this may exhibit fluorescence or other optical properties, which can be useful in various analytical applications.
Formula:C12H9NS
Synonyms:- 2-(2-Thienyl)-1H-indole
- 2-(2-Thienyl)indole
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Found 4 products.
2-(Thiophen-2-yl)-1H-indole
CAS:<p>2-(Thiophen-2-yl)-1H-indole is a reagent that can be used in the screening of potential anticancer drugs. The compound has been shown to inhibit the growth of cultured human cancer cells by inhibiting the synthesis of DNA. This inhibition is due to its ability to interact with hydrogen bonds and hydrophobic interactions, which are key players in biological activity. 2-(Thiophen-2-yl)-1H-indole is potent against tumor cells and has been shown to have antiangiogenic effects on endothelial cells. This compound also inhibits transcription, leading to an increased number of transcripts.</p>Formula:C12H9NSPurity:Min. 95%Molecular weight:199.27 g/mol
