structure of 24621-70-3

1H-Indole-2-Methanol

CAS No.: 24621-70-3 Brand: MolBest
M. Ft.: C9H9NO Cat. No: G5329713
M. Wt.: 147.17 MDL: No record
Storage: 2-8°C
Purity Grade Package Stock Price Quantity
97% RG 250MG In Stock 4 USD
97% RG 1G In Stock 6 USD
97% RG 5G In Stock 16 USD
97% RG 25G In Stock 50 USD
97% RG 500G In Stock 1346 USD
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Applications of 24621-70-3

1H-Indole-2-methanol finds applications across various fields:

  • Pharmaceuticals: It serves as a precursor for synthesizing biologically active compounds, particularly those targeting neurotransmitter systems.
  • Material Science: Its derivatives are explored for use in organic electronics and photonic devices due to their electronic properties.
  • Agriculture: Some indole derivatives are investigated for their potential as agrochemicals.

Biological Activity of 24621-70-3

1H-Indole-2-methanol exhibits notable biological activities, including:

  • Antimicrobial Properties: Studies have shown that derivatives of indole compounds possess significant antibacterial and antifungal activity. For instance, certain synthesized derivatives have demonstrated effectiveness against pathogens such as Staphylococcus aureus and Candida albicans .
  • CYP Enzyme Inhibition: This compound has been identified as a CYP1A2 inhibitor, which may influence drug metabolism and pharmacokinetics .
  • Neuropharmacological Effects: Some studies suggest that indole derivatives can interact with serotonin receptors, indicating potential applications in treating mood disorders and other neuropsychiatric conditions .

NMR spectrum of 24621-70-3

Physical sample testing spectrum (NMR) of 24621-70-3

Safety Information of 24621-70-3

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Signal Word

Danger

Hazard Statements

H318 Causes serious eye damage

Safety Data Sheet

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Bulk Packaging Price Explanation of 24621-70-3

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Purchase Instructions of 24621-70-3

All products are for research and development use only, not for any other uses, and must be handled by technically-qualified persons.

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