CAS 4837-74-5
:(4-methoxy-1H-indol-3-yl)acetonitrile
Description:
(4-Methoxy-1H-indol-3-yl)acetonitrile, with the CAS number 4837-74-5, is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. The presence of a methoxy group at the 4-position of the indole ring contributes to its unique properties, including potential solubility in organic solvents and influence on biological activity. The acetonitrile functional group introduces a nitrile (-C≡N) moiety, which can enhance the compound's reactivity and polarity. This compound may exhibit interesting pharmacological properties, making it of interest in medicinal chemistry and drug development. Its synthesis typically involves reactions that introduce the methoxy and acetonitrile groups onto the indole framework. As with many organic compounds, its stability, reactivity, and potential applications can be influenced by environmental conditions such as pH and temperature. Overall, (4-methoxy-1H-indol-3-yl)acetonitrile represents a versatile structure in organic synthesis and medicinal chemistry.
Formula:C11H10N2O
InChI:InChI=1/C11H10N2O/c1-14-10-4-2-3-9-11(10)8(5-6-12)7-13-9/h2-4,7,13H,5H2,1H3
SMILES:COc1cccc2c1c(CC#N)c[nH]2
Synonyms:- 1H-indole-3-acetonitrile, 4-methoxy-
- (4-Methoxy-1H-indol-3-yl)acetonitrile
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Found 4 products.
2-(4-Methoxy-1H-indol-3-yl)acetonitrile
CAS:Formula:C11H10N2OColor and Shape:SolidMolecular weight:186.20992-(4-Methoxy-1H-indol-3-yl)acetonitrile
CAS:<p>2-(4-Methoxy-1H-indol-3-yl)acetonitrile is a chemical compound that has been shown to have potent anti-inflammatory effects. It is a plant hormone that has been found in the leaves of many plant families, including members of the genus "Tussilago", which produce a class of phytoalexins called tussilagone. 2-(4-Methoxy-1H-indol-3-yl)acetonitrile binds to toll like receptor 4 and inhibits the production of proinflammatory cytokines such as tumor necrosis factor alpha (TNFα). This compound also inhibits dextran sulfate sodium induced lung damage and has been shown to be effective in animal models of inflammatory diseases.</p>Formula:C11H10N2OPurity:Min. 95%Color and Shape:PowderMolecular weight:186.21 g/mol2-(4-methoxy-1H-indol-3-yl)acetonitrile
CAS:Controlled Product<p>Applications 2-(4-methoxy-1H-indol-3-yl)acetonitrile (cas# 4837-74-5) is a useful research chemical.<br></p>Formula:C11H10N2OColor and Shape:NeatMolecular weight:186.2



