
CAS 61019-05-4
:5-methoxy-7-methyl-1H-Indole
Description:
5-Methoxy-7-methyl-1H-indole, with the CAS number 61019-05-4, is an organic compound belonging to the indole family, which is characterized by a bicyclic structure consisting of a six-membered benzene ring fused to a five-membered nitrogen-containing pyrrole ring. This compound features a methoxy group (-OCH3) at the 5-position and a methyl group (-CH3) at the 7-position of the indole structure, which can influence its chemical reactivity and biological activity. It is typically a solid at room temperature and may exhibit solubility in organic solvents. The presence of the methoxy and methyl substituents can enhance its lipophilicity, potentially affecting its interaction with biological systems. Indoles are known for their diverse pharmacological properties, including roles in neurotransmission and as precursors to various natural products. As with many indole derivatives, 5-methoxy-7-methyl-1H-indole may be of interest in medicinal chemistry and research related to neurobiology and other fields.
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Found 5 products.
5-Methoxy-7-methylindole, 97%
CAS:<p>5-Methoxy-7-methylindole is employed as a intermediate for chemical research and pharmaceutical. 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 pro</p>Formula:C10H11NOPurity:97%Molecular weight:161.25-Methoxy-7-Methylindole
CAS:Formula:C10H11NOPurity:98%Color and Shape:SolidMolecular weight:161.20045-Methoxy-7-methyl-1H-indole
CAS:Formula:C10H11NOPurity:98%Color and Shape:Liquid, No data available.Molecular weight:161.2045-Methoxy-7-methyl-1H-indole
CAS:<p>5-Methoxy-7-methyl-1H-indole is a synthetic molecule that acts as a potent agonist of the melatonin receptors. It has been shown to have an affinity for the 5HT2A receptor, and it is also an electronegative molecule. The potency of this compound has been shown in amphibian and human cells. 5-Methoxy-7-methyl-1H-indole has analogues which show different degrees of agonist potency and selectivity for the melatonin receptors. Substituents on the 5-methoxy group affect electropositive properties and affinity for melatonin receptors.</p>Formula:C10H11NOPurity:Min. 95%Molecular weight:161.2 g/mol




