N-(2-Methoxyphenyl)acetamide 

N-(2-Methoxyphenyl)acetamide is a compound that can have significant relevance to everyday life due to its potential pharmaceutical applications. This compound has been studied for its potential uses in pain relief and anti-inflammatory medications. Its ability to interact with specific receptors in the body may make it a valuable ingredient in future medications aimed at managing various health conditions. As such, continued research on N-(2-Methoxyphenyl)acetamide could ultimately lead to the development of more effective treatments for individuals in need of pain management or anti-inflammatory relief.

Table of Contents:

💡  Commercial Applications

N-(2-Methoxyphenyl)acetamide, also known as O-methoxyacetanilide, finds application in various commercial and industrial processes. It is commonly used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and dyes. Due to its versatile nature, this compound is also employed in the production of plasticizers and antioxidants for use in the plastics industry.

In the realm of drug and medication applications, N-(2-Methoxyphenyl)acetamide exhibits potential pharmacological activity. It has been studied for its analgesic and anti-inflammatory properties, making it a candidate for the development of pain relief medication. The compound’s ability to inhibit certain enzymes in the body also presents opportunities for its use in therapeutic treatments for various conditions.

Furthermore, N-(2-Methoxyphenyl)acetamide has shown promise as a corrosion inhibitor in industrial settings. By forming a protective film on metal surfaces, this compound helps prevent rust and degradation, prolonging the lifespan of machinery and equipment. In addition, its low toxicity and environmental compatibility make it a desirable choice for applications where regulatory compliance is essential.

⚗️  Chemical & Physical Properties

N-(2-Methoxyphenyl)acetamide is a white crystalline solid with a faint odor. Its appearance is similar to other organic compounds, and its odor is not particularly distinctive.

The molar mass of N-(2-Methoxyphenyl)acetamide is approximately 179.21 g/mol, and its density is around 1.15 g/cm³. These values are comparable to common food items, such as sugar and salt, in terms of molar mass and density.

N-(2-Methoxyphenyl)acetamide has a melting point of around 150-152°C and a boiling point of approximately 360-370°C. These values are higher than those of most common food items, such as butter and chocolate, which have lower melting and boiling points.

N-(2-Methoxyphenyl)acetamide is sparingly soluble in water and has a low viscosity. This differs from common food items, such as sugar and salt, which are highly soluble in water and have varying viscosities.

🏭  Production & Procurement

N-(2-Methoxyphenyl)acetamide is typically produced through a chemical reaction between 2-methoxyaniline and acetic anhydride. This process results in the formation of the desired product, N-(2-Methoxyphenyl)acetamide, which can then be isolated and purified through standard laboratory techniques.

The procurement of N-(2-Methoxyphenyl)acetamide can be accomplished through chemical suppliers who specialize in providing fine chemicals and research reagents. Once procured, the compound can be transported in sealed containers to ensure its quality and stability during transit. Proper handling and storage procedures should be followed to maintain the integrity of the product.

Alternatively, N-(2-Methoxyphenyl)acetamide can also be synthesized in-house by research laboratories and pharmaceutical companies with the necessary expertise in organic synthesis. This allows for greater control over the quality and purity of the compound, as well as the ability to tailor the synthesis process to specific research or production requirements.

⚠️  Safety Considerations

Safety Considerations for N-(2-Methoxyphenyl)acetamide:

When handling N-(2-Methoxyphenyl)acetamide, it is important to wear appropriate personal protective equipment such as gloves, goggles, and lab coat to prevent skin and eye contact. The compound should be stored in a cool, dry, well-ventilated area away from direct sunlight and incompatible materials. In case of accidental exposure, immediately rinse affected area with plenty of water and seek medical attention if necessary.

Hazard Statements for N-(2-Methoxyphenyl)acetamide:

N-(2-Methoxyphenyl)acetamide may cause skin irritation and serious eye damage. It is harmful if swallowed and may be harmful if inhaled. Avoid breathing in dust or mist and avoid contact with skin and eyes. Keep the compound away from heat, sparks, and open flames.

Precautionary Statements for N-(2-Methoxyphenyl)acetamide:

When handling N-(2-Methoxyphenyl)acetamide, wear protective gloves, clothing, and eye protection. In case of skin contact, wash with plenty of soap and water. In case of eye contact, rinse cautiously with water for several minutes. If swallowed, seek medical advice immediately and show the container or label. Store in a well-ventilated place away from heat and sources of ignition.

🔬  Potential Research Directions

One potential research direction for N-(2-Methoxyphenyl)acetamide is its pharmaceutical applications, particularly in the development of novel analgesics or anti-inflammatory drugs. Its structural similarity to other known pharmaceutical compounds may lend itself to investigation as a potential drug lead.

Another avenue of research could explore the chemical synthesis and characterization of derivatives of N-(2-Methoxyphenyl)acetamide. By modifying the structure of the compound, researchers may uncover new properties or activities that could be harnessed for various applications.

Furthermore, studies focusing on the biological activity and mechanism of action of N-(2-Methoxyphenyl)acetamide could provide valuable insights into its potential therapeutic benefits. Understanding how the compound interacts with biological systems could lead to the development of more targeted and effective treatments.

One similar compound to N-(2-Methoxyphenyl)acetamide based upon molecular structure is N-(3-Methoxyphenyl)acetamide. In this compound, the methoxy group is attached to the phenyl ring at the 3-position instead of the 2-position, while the acetamide group remains the same. This slight modification in the position of the methoxy group can lead to differences in properties and activities compared to N-(2-Methoxyphenyl)acetamide.

Another similar compound is N-(4-Methoxyphenyl)acetamide. In this compound, the methoxy group is attached to the phenyl ring at the 4-position, while the acetamide group remains constant. Just like N-(3-Methoxyphenyl)acetamide, the positioning of the methoxy group at a different position on the phenyl ring can result in variations in the compound’s characteristics and behavior.

A further related compound is N-(2-Hydroxyphenyl)acetamide. In this compound, the methoxy group is replaced with a hydroxy group on the phenyl ring, while the acetamide group remains unchanged. The presence of a hydroxy group instead of a methoxy group can lead to significant differences in the compound’s properties and biological activities. This compound showcases the impact of small modifications in molecular structure on the overall behavior of the compound.

Previous Post

Phenanthren-2-ol

Next Post

Albendazole

You cannot copy content of this page