CAS 202584-22-3
:6-(Methylthio)-1H-indole
Description:
6-(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 6-position of the indole ring contributes to its unique chemical properties. This compound is typically a solid at room temperature and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The methylthio group can influence the compound's solubility, reactivity, and interaction with biological targets. Additionally, 6-(Methylthio)-1H-indole may exhibit fluorescence properties, making it useful in various analytical applications. Its synthesis often involves methods such as nucleophilic substitution or cyclization reactions. As with many indole derivatives, it may also participate in various chemical reactions, including electrophilic aromatic substitution, which can be exploited for further functionalization. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.
Formula:C9H9NS
InChI:InChI=1S/C9H9NS/c1-11-8-3-2-7-4-5-10-9(7)6-8/h2-6,10H,1H3
InChI key:InChIKey=XBTHQAKYJGTLRT-UHFFFAOYSA-N
SMILES:S(C)C=1C=C2C(=CC1)C=CN2
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Found 2 products.
6-(Methylsulfanyl)-1H-indole
CAS:<p>6-(Methylsulfanyl)-1H-indole is a potent cox-2 inhibitor that has been shown to selectively inhibit cyclooxygenase-2, which is the enzyme responsible for the conversion of arachidonic acid to prostaglandins. This drug has been shown to be effective in reducing inflammation by inhibiting the production of prostaglandins and leukotrienes. 6-(Methylsulfanyl)-1H-indole also has a hydrophilic conformation that allows it to have greater selectivity for COX-2 than other drugs, such as celecoxib.</p>Formula:C9H9NSPurity:Min. 95%Molecular weight:163.24 g/mol
