CAS 53330-94-2

1-(1H-Indol-5-yl)ethanone

Description:

1-(1H-Indol-5-yl)ethanone, also known as indole-5-ethanone, is an organic compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features a ketone functional group (ethanone) attached to the indole at the 5-position. It typically appears as a solid or crystalline substance and is known for its aromatic properties, contributing to its potential applications in pharmaceuticals and organic synthesis. The presence of the indole moiety suggests that it may exhibit biological activity, as many indole derivatives are known for their roles in medicinal chemistry. The compound is soluble in organic solvents, and its reactivity can be influenced by the electron-rich nature of the indole ring. Safety data should be consulted for handling, as with any chemical substance, to ensure proper precautions are taken. Overall, 1-(1H-Indol-5-yl)ethanone is of interest in various fields, including drug development and materials science.

Formula: C₁₀H₉NO

InChI: InChI=1/C10H9NO/c1-7(12)8-2-3-10-9(6-8)4-5-11-10/h2-6,11H,1H3

InChI key: InChIKey=GOFIUEUUROFVMA-UHFFFAOYSA-N

SMILES: C(C)(=O)C=1C=C2C(=CC1)NC=C2

Synonyms:

• 1-(1H-Indol-5-yl)ethan-1-one
• 1-(1H-Indol-5-yl)ethanone
• 5-Acetyl-1H-indole
• Ethanone, 1-(1H-indol-5-yl)-
• Ketone, indol-5-yl methyl
• 5-Acetylindole
• Ethanone, 1-(1H-indol-5-yl)-(9CI)
• ketone,indol-5-ylmethyl
• 5-ACETYLINDOLE 97+%
• 5-INDOLYL-METHYLKETONE

5-Acetyl-1H-indole

CAS: 53330-94-2

5-Acetyl-1H-indole

Formula: C₁₀H₉NO

Purity: 99%

Color and Shape: Solid

Molecular weight: 159.18456

Ref: 54-OR8356

1-(1H-Indol-5-yl)ethanone

CAS: 53330-94-2

Formula: C₁₀H₉NO

Purity: 97%

Color and Shape: Solid

Molecular weight: 159.1846

Ref: IN-DA003915

5-Acetylindole

CAS: 53330-94-2

5-Acetylindole is a synthetic compound that has been shown to have anticancer activity. It inhibits the growth of cancer cells by disrupting their mitochondria, which leads to cell death. 5-Acetylindole was synthesized in an attempt to increase the anticancer efficacy of indole compounds and acetylation of indole rings was found to be an effective strategy for this purpose. Acetylation of the 5 position on the indole ring leads to a more potent antiproliferative agent with decreased potential for resistance development. This compound has been shown to disrupt cellular function in k562 cells, leading to cell death.

Formula: C₁₀H₉NO

Purity: Min. 95%

Molecular weight: 159.18 g/mol

Ref: 3D-FA52333

1-(1H-Indol-5-yl)-ethanone

CAS: 53330-94-2

Formula: C₁₀H₉NO

Purity: 97%

Color and Shape: Solid, Powder

Molecular weight: 159.188

Ref: 10-F040212