1H-Indole, 2-ethoxy- is an organic compound characterized by its indole structure, which consists of a fused benzene and pyrrole ring. This compound features an ethoxy group (-OCH2CH3) attached to the second position of the indole ring, influencing its chemical properties and reactivity. It is typically a colorless to pale yellow liquid with a distinctive odor. The presence of the ethoxy group enhances its solubility in organic solvents while potentially affecting its biological activity. 1H-Indole derivatives are known for their diverse applications in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. The compound may exhibit various functional properties, including potential antimicrobial or anti-inflammatory activities, depending on its specific structure and substituents. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Overall, 1H-Indole, 2-ethoxy- is a significant compound in the realm of organic chemistry with potential utility in various fields.

1H-Indole, 2-ethoxy-

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2-Ethoxy-1H-indole is a synthetic, nucleophilic compound that has been shown to be an effective hydrogenation catalyst. The biological properties of 2-ethoxy-1H-indole have been studied in both animals and humans. In rats, this compound has shown to be an effective analgesic and antiinflammatory agent with few side effects. 2-Ethoxy-1H-indole also has shown efficacy in the treatment of Parkinson's disease in animal models. This drug can be used as a precursor for a variety of compounds including carboximidamides, enecarbamates, amines, or sulfoxides. It is also possible to control the stereocontrol of 2-ethoxy-1H-indole by using chiral reagents or by converting it to its chiral counterpart (2-(2'-ethoxy)-1H-indole).

CAS 1009-27-4: 1H-Indole, 2-ethoxy-

1H-Indole, 2-ethoxy-

Ref: IN-DA00034T

2-Ethoxy-1H-indole

Ref: 3D-BAA00927

2-Ethoxy-1H-indole

Ref: 10-F626733