CAS 66440-60-6

1,5-dimethyl-1H-indole-2,3-dione

Description:

1,5-Dimethyl-1H-indole-2,3-dione, with the CAS number 66440-60-6, is a chemical compound characterized by its indole structure, which is a bicyclic compound consisting of a benzene ring fused to a pyrrole ring. This compound features two methyl groups at the 1 and 5 positions of the indole ring and two carbonyl groups at the 2 and 3 positions, contributing to its diketone nature. The presence of these functional groups imparts unique chemical reactivity, making it a potential candidate for various synthetic applications in organic chemistry. It may exhibit properties such as fluorescence or biological activity, depending on its specific interactions with other molecules. Additionally, its solubility and stability can vary based on the solvent and environmental conditions. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks or environmental hazards. Overall, 1,5-dimethyl-1H-indole-2,3-dione is of interest in both academic research and potential industrial applications.

Formula: C₁₀H₉NO₂

InChI: InChI=1/C10H9NO2/c1-6-3-4-8-7(5-6)9(12)10(13)11(8)2/h3-5H,1-2H3

SMILES: Cc1ccc2c(c1)C(=O)C(=O)N2C

Synonyms:

• 1,5-Dimethylisatin
• 1H-indole-2,3-dione, 1,5-dimethyl-
• 1,5-Dimethyl-1H-indole-2,3-dione

1,5-Dimethylindoline-2,3-dione

CAS: 66440-60-6

Formula: C₁₀H₉NO₂

Purity: 98%

Molecular weight: 175.1840

Ref: IN-DA00FD9Y

1,5-Dimethyl-2,3-dihydro-1h-indole-2,3-dione

CAS: 66440-60-6

1,5-Dimethyl-2,3-dihydro-1h-indole-2,3-dione

Purity: 98%

Molecular weight: 175.18g/mol

Ref: 54-OR91393

1,5-Dimethyl-1H-indole-2,3-dione

CAS: 66440-60-6

Formula: C₁₀H₉NO₂

Purity: 98%

Molecular weight: 175.187

Ref: 10-F060413

1,5-Dimethyl-1H-indole-2,3-dione

CAS: 66440-60-6

1,5-Dimethyl-1H-indole-2,3-dione is a molecule with antibacterial activity. It has been shown to have interactions with staphylococcus and subtilis strains. Computational results show that the molecule has inhibitory effects on bacterial dna gyrase and topoisomerase IV. This inhibits the synthesis of bacterial proteins and leads to cell death. Hydrazides have been shown to be effective against staphylococcus aureus isolates and are hypothesized to inhibit protein synthesis by binding to bacterial ribosomes. The mechanism of action of 1,5-dimethyl-1H-indole-2,3-dione is not yet known.

Formula: C₁₀H₉NO₂

Purity: Min. 95%

Molecular weight: 175.19 g/mol

Ref: 3D-RCA44060