3-Methyloxindole

3-Methyloxindole is a compound that plays a crucial role in various biological processes, including the synthesis of serotonin in the brain and the regulation of gut motility. This compound has been the subject of research in the medical and pharmaceutical fields due to its potential therapeutic applications in treating mood disorders and gastrointestinal issues. Understanding the functions and effects of 3-Methyloxindole can provide valuable insights into the mechanisms underlying certain physiological and psychological conditions, ultimately contributing to the development of novel treatments and improving overall quality of life.

Table of Contents:

💡  Commercial Applications

3-Methyloxindole, a chemical compound with the molecular formula C9H9NO, finds various commercial and industrial applications. It is commonly used in the synthesis of pharmaceutical drugs, such as anti-inflammatory agents and antibiotics. Additionally, 3-Methyloxindole is employed in the production of agrochemicals and dyes due to its versatile chemical properties.

In the realm of drug and medication applications, 3-Methyloxindole plays a crucial role as a key intermediate in the synthesis of certain medications. Due to its structural features, this compound is utilized in the pharmaceutical industry to develop biologically active compounds with potential therapeutic benefits. Moreover, 3-Methyloxindole serves as a valuable building block for creating novel drug molecules that target specific biological pathways and cellular processes.

Furthermore, 3-Methyloxindole is known for its potential pharmacological activities, making it a promising candidate for drug discovery and development. Research has shown that this compound exhibits anti-cancer properties by inhibiting the growth of cancer cells through various mechanisms. Additionally, studies have suggested that 3-Methyloxindole may have neuroprotective effects, making it a topic of interest in the field of neuroscience for potential therapeutic interventions against neurodegenerative diseases.

⚗️  Chemical & Physical Properties

3-Methyloxindole is a white crystalline solid with a faint, odor reminiscent of indole. Its appearance is often described as powdery or granular.

The molar mass of 3-Methyloxindole is approximately 147.16 g/mol, and its density is 1.19 g/cm^3. Compared to common food items, 3-Methyloxindole has a higher molar mass and density, making it a relatively dense compound.

3-Methyloxindole has a melting point of 103-105°C and a boiling point of 282°C. In comparison to common food items, 3-Methyloxindole has higher melting and boiling points, indicating its stability at higher temperatures.

3-Methyloxindole has a limited solubility in water and is relatively viscous in its pure form. Compared to common food items, 3-Methyloxindole exhibits lower solubility in water and higher viscosity, making it less suitable for aqueous solutions.

🏭  Production & Procurement

3-Methyloxindole is typically produced through a multistep synthesis reaction using starting materials such as indole and 3-methylacrylic acid. This reaction sequence involves several chemical steps, including an esterification, cyclization, and decarboxylation, ultimately yielding the desired 3-Methyloxindole product.

In order to procure 3-Methyloxindole, one can either synthesize it in a laboratory setting following the aforementioned production method or purchase it from chemical suppliers. The compound can be transported as a solid powder or dissolved in a solvent for easier handling and storage. Care must be taken to ensure proper handling and storage of 3-Methyloxindole to prevent degradation or contamination.

When procuring 3-Methyloxindole for research or industrial purposes, it is important to verify the purity and quality of the compound from the supplier. This can be done through various analytical techniques such as spectroscopy or chromatography. Additionally, proper documentation and labeling should accompany the shipment of 3-Methyloxindole to ensure traceability and regulatory compliance.

⚠️  Safety Considerations

Safety considerations for 3-Methyloxindole should be taken into account due to its potential hazards. This compound is flammable and may cause irritation to the skin, eyes, and respiratory system upon contact. It is important to handle 3-Methyloxindole with caution, using appropriate personal protective equipment such as gloves and goggles to prevent exposure. Additionally, proper ventilation should be ensured when working with this compound to minimize the risk of inhalation.

Hazard statements for 3-Methyloxindole include: “Causes skin irritation,” “Causes serious eye irritation,” and “May cause respiratory irritation.” These statements highlight the potential health risks associated with exposure to this compound. It is important to be aware of these hazards and take appropriate precautions to prevent any adverse effects.

Precautionary statements for 3-Methyloxindole include: “Avoid breathing dust/fume/gas/mist/vapors/spray,” “Wear protective gloves/protective clothing/eye protection/face protection,” and “Wash hands thoroughly after handling.” These statements emphasize the importance of taking necessary precautions to minimize the risk of exposure to 3-Methyloxindole and protect against potential health hazards. By following these guidelines, individuals can safely handle and work with this compound.

🔬  Potential Research Directions

Potential research directions of 3-Methyloxindole include investigating its role as a bio-active compound in pharmaceutical applications, particularly in the development of novel drugs for various diseases. Researchers could explore its interaction with biological targets and potential pathways for therapeutic interventions.

Furthermore, studies could focus on elucidating the chemical properties of 3-Methyloxindole and its potential applications in organic synthesis and material science. Researchers may investigate its reactivity with other molecules and its potential for serving as a building block in the synthesis of complex organic compounds.

Lastly, research could delve into the environmental impact of 3-Methyloxindole, including its presence in pollutants and its potential toxicity to living organisms. Studies could explore its degradation pathways in the environment and its potential effects on ecosystems. Additionally, researchers could investigate methods for detecting and mitigating its presence in environmental samples.

One similar compound to 3-Methyloxindole based upon molecular structure is 2-Methyloxindole, which is a derivative of oxindole with a methyl group attached at the 2-position instead of the 3-position. This alteration in the position of the methyl group can lead to different biochemical, pharmacological, and physiological properties compared to 3-Methyloxindole. The structural similarity between these two compounds allows for comparison in terms of their bioactivity and potential applications in various fields of research.

Another related compound to 3-Methyloxindole is 3-Ethyl-2-oxindole, where an ethyl group is substituted at the 3-position of the oxindole ring. This structural modification can influence the compound’s reactivity, stability, and interaction with other molecules compared to 3-Methyloxindole. Understanding the similarities and differences between these compounds based on their molecular structures is crucial for elucidating their biological activities and potential therapeutic uses in medicine.

Furthermore, 4-Methyloxindole is a compound that shares a similar oxindole core structure with 3-Methyloxindole but with a methyl group attached at the 4-position. This subtle change in the substitution pattern can impact the compound’s chemical reactivity, solubility, and binding affinity to biological targets. Exploring the similarities and differences between 4-Methyloxindole and 3-Methyloxindole can provide valuable insights into the structure-activity relationships of oxindole derivatives and their potential applications in drug discovery and development.

Previous Post

4'-Hydroxyacetophenone 

Next Post

4-Methylbenzoic acid 

You cannot copy content of this page