84354-17-6 Usage
Description
5-(Benzyloxy)-2-Methoxyphenol is an antioxidant phenolic compound characterized by its benzyloxy and methoxy functional groups attached to a phenol backbone. It exhibits strong antioxidant properties, which can be attributed to its molecular structure and the presence of quantum chemical descriptors.
Uses
Used in Pharmaceutical Industry:
5-(Benzyloxy)-2-Methoxyphenol is used as a pharmaceutical agent for its potent antioxidant capabilities. It can help in the development of drugs that target oxidative stress-related diseases and conditions, such as neurodegenerative disorders, cardiovascular diseases, and cancer.
Used in Cosmetic Industry:
In the cosmetic industry, 5-(Benzyloxy)-2-Methoxyphenol is used as an antioxidant ingredient in skincare and beauty products. Its ability to neutralize free radicals and protect against oxidative damage makes it an effective component in formulations designed to maintain skin health, prevent premature aging, and improve overall skin appearance.
Used in Food and Beverage Industry:
5-(Benzyloxy)-2-Methoxyphenol is utilized as a natural antioxidant in the food and beverage industry to extend the shelf life of products and protect them from spoilage. It can be incorporated into various food products, such as processed meats, oils, and beverages, to prevent oxidation and maintain freshness.
Used in Nutraceutical Industry:
5-(Benzyloxy)-2-Methoxyphenol is employed as a nutraceutical ingredient to support overall health and well-being. It can be found in dietary supplements and functional foods that aim to provide antioxidant benefits, promote a healthy immune system, and reduce the risk of chronic diseases.
Used in Research and Development:
5-(Benzyloxy)-2-Methoxyphenol is also used in research and development for the study of its antioxidant properties and potential applications in various fields. It serves as a valuable compound for scientists to investigate its mechanisms of action, interactions with other molecules, and possible synergistic effects with other antioxidants.
Check Digit Verification of cas no
The CAS Registry Mumber 84354-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,3,5 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 84354-17:
(7*8)+(6*4)+(5*3)+(4*5)+(3*4)+(2*1)+(1*7)=136
136 % 10 = 6
So 84354-17-6 is a valid CAS Registry Number.
84354-17-6Relevant articles and documents
Facile synthesis of polyhydroxycoumaronochromones with quinones: Synthesis of alkylpolyhydroxy- and alkoxycoumaronochromones from 2′-hydroxyisoflavones
Tsukayama, Masao,Oda, Akihiro,Kawamura, Yasuhiko,Nishiuchi, Masaki,Yamashita, Kazuyo
, p. 6163 - 6166 (2007/10/03)
4′,5,7-Trihydroxy- or 8-alkyl-4′,5,7-trihydroxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2′-hydroxyisoflavones with o-chloranil under mild conditions. By contrast, alkoxycoumaronochromones were synthesized by oxidative cyclization of the corresponding 2′-hydroxyisoflavones with DDQ.
