7-Methoxy-5-methyl-2-phenylchromen-4-one

7-Methoxy-5-methyl-2-phenylchromen-4-one, also known as Isopsoralen, is a naturally occurring compound found in certain plants such as psoralea corylifolia and bergamot. This compound has demonstrated potential biological activities, including anti-inflammatory, antioxidant, anti-cancer, and antimicrobial properties. In everyday life, Isopsoralen may have implications for skincare products, dietary supplements, and pharmaceuticals due to its possible health benefits. Further research into its effects and applications could lead to new developments in health and wellness products.

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💡  Commercial Applications

7-Methoxy-5-methyl-2-phenylchromen-4-one, also known as apigenin, has several commercial and industrial applications. It is commonly used as a natural dye in the textile industry due to its yellow color. Additionally, apigenin is used in the production of certain cosmetics and skincare products for its antioxidant properties.

In the realm of drug and medication applications, apigenin has shown potential as a natural remedy for various health conditions. It has anti-inflammatory properties and may help reduce inflammation in the body. Apigenin has also been studied for its potential anti-cancer effects, as it has been shown to inhibit the growth of cancer cells in some studies.

Furthermore, apigenin has been used in traditional medicine for its sedative and anxiolytic effects. It is believed to have calming properties that can help reduce anxiety and promote relaxation. Apigenin may also have benefits for cardiovascular health, as studies have shown it may help lower blood pressure and reduce the risk of heart disease.

⚗️  Chemical & Physical Properties

7-Methoxy-5-methyl-2-phenylchromen-4-one is a white crystalline powder with a faint odor. It has a characteristic sweet aroma that is subtle yet distinct.

The molar mass of 7-Methoxy-5-methyl-2-phenylchromen-4-one is approximately 284.3 g/mol, with a density of about 1.3 g/cm3. Compared to common food items, this compound has a higher molar mass and density than most organic molecules found in food.

The compound has a melting point of around 150-152°C and a boiling point of approximately 334-336°C. These values are considerably higher than those of many common food items, which typically have melting and boiling points well below 100°C.

7-Methoxy-5-methyl-2-phenylchromen-4-one is sparingly soluble in water and tends to form a viscous solution. This compound’s solubility in water and viscosity are much lower than many common food items, which are often highly soluble and have low viscosity in aqueous solutions.

🏭  Production & Procurement

7-Methoxy-5-methyl-2-phenylchromen-4-one is typically produced through a multi-step synthesis process in a laboratory setting. Starting materials such as methyl ketone and substituted phenol are reacted under specific conditions to form the desired compound.

Once synthesized, 7-Methoxy-5-methyl-2-phenylchromen-4-one can be procured from specialized chemical suppliers who produce and distribute organic compounds for research and industrial purposes. The compound is typically sold in solid form and can be transported in sealed containers to ensure its purity.

Transportation of 7-Methoxy-5-methyl-2-phenylchromen-4-one is usually carried out using standard chemical shipping methods to prevent any degradation or contamination during transit. Proper labeling and packaging are essential to ensure compliance with regulations governing the transportation of hazardous materials.

⚠️  Safety Considerations

Safety considerations for 7-Methoxy-5-methyl-2-phenylchromen-4-one, commonly known as Coumarin, must be taken seriously due to its potential hazards. The compound has been classified as harmful if swallowed, inhaled, or in contact with the skin. It may cause irritation to the respiratory system if inhaled and may cause skin irritation upon contact. Additionally, it has been found to be harmful to aquatic life with long-lasting effects.

Hazard statements for 7-Methoxy-5-methyl-2-phenylchromen-4-one highlight its potential dangers. These include causing irritation to the skin, eyes, and respiratory system upon contact or inhalation. The compound is also harmful if swallowed and may have adverse effects on aquatic life. It is important to handle this substance with caution and take necessary safety measures to prevent any harm.

Precautionary statements for handling 7-Methoxy-5-methyl-2-phenylchromen-4-one emphasize the importance of avoiding inhalation, skin, and eye contact. It is recommended to use appropriate protective clothing, gloves, and eye protection when handling this compound. In case of exposure, it is advised to seek medical attention and rinse affected areas thoroughly with water. Additionally, proper disposal methods should be followed to prevent environmental contamination.

🔬  Potential Research Directions

One potential research direction for 7-Methoxy-5-methyl-2-phenylchromen-4-one is its investigation as a potential therapeutic agent for various medical conditions. Studies could focus on its pharmacological properties, including its anti-inflammatory, anti-cancer, or antioxidant effects.

Another avenue of research could involve exploring the potential synthesis of analogs or derivatives of 7-Methoxy-5-methyl-2-phenylchromen-4-one to enhance its biological activity or improve its pharmacokinetic profile. This could lead to the development of novel drug candidates with improved efficacy and safety profiles.

Furthermore, research efforts could be directed towards elucidating the mechanism of action of 7-Methoxy-5-methyl-2-phenylchromen-4-one at a molecular level. Understanding how this compound interacts with its biological targets could provide valuable insights into its therapeutic potential and help guide the design of more potent and selective compounds.

One similar compound to 7-Methoxy-5-methyl-2-phenylchromen-4-one is 5-Methoxy-7-methyl-2-phenylchromen-4-one. This compound differs in the position of the methoxy and methyl groups compared to the original compound. The rearrangement of these groups may result in differences in the compound’s biological activity or chemical properties.

Another similar compound is 7-Hydroxy-5-methyl-2-phenylchromen-4-one. In this compound, the methoxy group has been replaced with a hydroxy group, altering its polarity and potential interactions with other molecules. This change may have implications for the compound’s solubility or reactivity in specific environments.

A third related compound is 7-Methoxy-5-ethyl-2-phenylchromen-4-one. Here, the methyl group of the original compound has been replaced with an ethyl group, leading to differences in molecular size and possibly in flexibility. The introduction of the ethyl group may impact the compound’s binding affinity or stability with target proteins.

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