• 1. Dual effects of cardamonin/alpinetin and their acrolein adducts on scavenging acrolein and the anti-bacterial activity from Alpinia katsumadai Hayata as a spice in roasted meat
  Yang Lu,Juan Liu,Jiaqi Tong,Chenxiao Zhang,Yi Duan,Xiaoli Song,Yongling Lu,Lishuang Lv Food Funct. 2022 13 7088
• 2. Amomum subulatum mitigates experimental thoracic radiation-induced lung injury by regulating antioxidant status and inflammatory responses
  Sudarsanan Drishya,Suresh Sulekha Dhanisha,Paramu Raghukumar,Chandrasekharan Guruvayoorappan Food Funct. 2023 14 1545
• 3. Notes
  N. Pravdi?,D. Keglevi?,E. D. Andrews,W. E. Harvey,Roger Bolton,A. F. Casy,J. L. Myers,D. W. Mathiwson,W. B. Whalley,J. M. Blatchly,R. Taylor,A. B. A. Jansen,P. J. Stokes,G. W. H. Cheeseman,J. S. Davidson,J. M. Crabtree,P. N. Gates,E. F. Mooney,J. K. Sutherland,D. A. Widdowson,Stang Mongkolsuk,F. M. Dean,G. W. Kirby,H. P. Tiwari,D. J. Machin,D. F. C. Morris,E. L. Short,R. S. Bluck,A. L. Odell,R. W. Olliff,J. Burdon,W. B. Hollyhead,C. R. Patrick,J. A. Salthouse,T. C. Waddington,Shreekrishna M. Gadedar,Anna Marie Kotsen,Elliott Cohen J. Chem. Soc. 1964 4633
• 4. Non-covalent interaction of dietary polyphenols with total plasma proteins of type II diabetes: molecular structure/property–affinity relationships
  Jianbo Xiao,Yaru Zhao,Hui Wang,Yongming Yuan,Fan Yang,Chao Zhang,Guoyin Kai Integr. Biol. 2011 3 1087
• 5. Natural and synthetic flavonoid derivatives as new potential tyrosinase inhibitors: a systematic review
  Rami J. Obaid,Ehsan Ullah Mughal,Nafeesa Naeem,Amina Sadiq,Reem I. Alsantali,Rabab S. Jassas,Ziad Moussa,Saleh A. Ahmed RSC Adv. 2021 11 22159

• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Flavonoids 5-O-methylated flavonoids
• Solvents and Organic Chemicals Organic Compounds Phenylpropanoids and polyketides Flavonoids O-methylated flavonoids 5-O-methylated flavonoids
• Natural Products and Extracts Plant Extracts Plant based Fridericia triplinervia
• Pharmaceutical and Biochemical Products Pharmaceutical Active Ingredients Standard Substances

Exploring the Properties and Applications of 7-Hydroxy-5-methoxy-2-phenylchroman-4-one (CAS No. 1090-65-9)

7-Hydroxy-5-methoxy-2-phenylchroman-4-one, with the CAS number 1090-65-9, is a naturally occurring flavonoid derivative that has garnered significant attention in both scientific and industrial communities. This compound, often referred to as a chromanone derivative, exhibits unique structural features that contribute to its diverse biological activities and potential applications. Researchers have been particularly interested in its antioxidant properties and possible health benefits, making it a subject of numerous studies in recent years.

The molecular structure of 7-Hydroxy-5-methoxy-2-phenylchroman-4-one consists of a chroman-4-one core with specific substitutions at the 2, 5, and 7 positions. The presence of both hydroxy and methoxy groups in its structure contributes to its polarity and solubility characteristics. These structural elements are crucial for its bioactivity and have been the focus of structure-activity relationship studies. The compound's molecular weight and logP value make it particularly interesting for pharmaceutical research and development.

Recent studies have highlighted the potential of 7-Hydroxy-5-methoxy-2-phenylchroman-4-one in various applications. Its antioxidant capacity has been compared to other well-known flavonoids, with some research suggesting it may have superior free radical scavenging activity. This property has sparked interest in its potential use in cosmetic formulations and nutraceutical products, especially in the context of anti-aging and skin protection applications. The compound's stability under different conditions is currently being investigated to determine its suitability for various product formulations.

The synthesis and extraction methods for 7-Hydroxy-5-methoxy-2-phenylchroman-4-one have evolved significantly in recent years. While it can be isolated from certain plant sources, most commercial production now utilizes synthetic pathways to ensure consistency and scalability. The optimization of these synthetic routes has been a hot topic in organic chemistry circles, with particular focus on improving yield and purity. Analytical techniques such as HPLC and mass spectrometry are routinely employed to characterize and quantify this compound in various matrices.

In the pharmaceutical sector, 7-Hydroxy-5-methoxy-2-phenylchroman-4-one has shown promise in preliminary studies for various therapeutic applications. Its potential anti-inflammatory effects and possible neuroprotective properties are currently under investigation. Researchers are particularly interested in its mechanism of action at the molecular level, with some studies suggesting it may interact with specific cellular signaling pathways. However, it's important to note that much of this research is still in early stages, and clinical applications would require extensive further study.

The market for chromanone derivatives like 7-Hydroxy-5-methoxy-2-phenylchroman-4-one has been growing steadily, driven by increasing demand for natural-derived compounds with potential health benefits. Industry analysts note particular interest from the cosmeceutical and dietary supplement sectors. The compound's relative stability compared to some other flavonoids makes it attractive for product formulation, though challenges remain in terms of bioavailability optimization and delivery systems.

Quality control and standardization of 7-Hydroxy-5-methoxy-2-phenylchroman-4-one preparations have become important topics as interest in this compound grows. Various analytical methods have been developed to ensure product consistency, with particular attention to impurity profiling and stability testing. Regulatory considerations for products containing this compound vary by region and intended use, creating an evolving landscape that manufacturers must navigate carefully.

Future research directions for 7-Hydroxy-5-methoxy-2-phenylchroman-4-one are likely to focus on several key areas. These include further elucidation of its biological mechanisms, development of more efficient synthetic methods, and exploration of novel applications in material science and other fields. The compound's potential role in green chemistry initiatives is also being examined, particularly in relation to its natural origins and biodegradability profile.

For researchers and industry professionals working with 7-Hydroxy-5-methoxy-2-phenylchroman-4-one, proper handling and storage recommendations should be followed to maintain compound integrity. While not classified as hazardous, standard laboratory precautions for organic compounds apply. The compound's solubility characteristics and stability under various conditions should be considered when designing experiments or formulations.

As interest in naturally-derived bioactive compounds continues to grow, 7-Hydroxy-5-methoxy-2-phenylchroman-4-one (CAS 1090-65-9) represents an interesting example of how traditional phytochemicals can find new applications in modern science and industry. Its unique combination of structural features and biological activities makes it a compound worth watching in coming years, particularly as research uncovers more about its potential benefits and applications across different sectors.

• 520-33-2(Hesperetin)
• 552-58-9(Eriodictyol)
• 487-26-3(Flavanone)
• 4250-77-5(6-Hydroxyflavanone)
• 578-86-9(Liquiritigenin)
• 24211-30-1(Farrerol)
• 36052-37-6(Alpinetin)
• 480-37-5(Pinostrobin)
• 480-41-1(Naringenin)
• 3034-04-6(6-Methoxy-2-phenyl-2,3-dihydrochromen-4-one)