CAS 40015-10-9
:3-(Methylthio)-1H-indole
Description:
3-(Methylthio)-1H-indole is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. The presence of a methylthio group at the 3-position of the indole ring contributes to its unique chemical properties. This compound is typically a solid at room temperature and may exhibit a range of solubility in organic solvents, depending on the specific conditions. It is known for its potential biological activity, which may include roles in medicinal chemistry and as a building block in the synthesis of various pharmaceuticals. The methylthio group can influence the compound's reactivity and interaction with biological targets. Additionally, 3-(Methylthio)-1H-indole may participate in various chemical reactions, such as electrophilic substitutions, due to the electron-rich nature of the indole ring. Its CAS number, 40015-10-9, is a unique identifier used for regulatory and safety purposes in chemical databases. As with many indole derivatives, it may also exhibit fluorescence properties, making it of interest in various analytical applications.
Formula:C9H9NS
InChI:InChI=1S/C9H9NS/c1-11-9-6-10-8-5-3-2-4-7(8)9/h2-6,10H,1H3
InChI key:InChIKey=TVHHOXFINVVIIT-UHFFFAOYSA-N
SMILES:S(C)C=1C=2C(NC1)=CC=CC2
Synonyms:- 3-(Methylthio)indole
- 1H-Indole, 3-(methylthio)-
- 3-(Methylthio)-1H-indole
- 3-Methylsulfanyl-1H-indole
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Found 1 products.
3-(Methylsulfanyl)-1H-indole
CAS:<p>3-(Methylsulfanyl)-1H-indole is a heterocyclic compound that contains a methylsulfanyl group. It is an orally active oxidant and thermally reactive molecule with a carbazole-like structure. 3-(Methylsulfanyl)-1H-indole undergoes oxidation in the presence of chloride ions to form sulfoxide, which can be reversibly converted back to the original compound by addition of hydrogen sulfide. The hypervalent character of this compound makes it switchable between two different oxidation states. 3-(Methylsulfanyl)-1H-indole has been shown to react with sulfoxides, such as dibenzothiophene-4,5-dithiol, to form products in which the sulfur atom is present in high oxidation states.</p>Formula:C9H9NSPurity:Min. 95%Molecular weight:163.24 g/mol
