174023-48-4 Usage
Description
3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one is a chemical compound belonging to the class of flavonoids, specifically a type of flavanone glycoside. It is characterized by the presence of two hydroxyl groups at the 3rd and 9th positions, and a pyran ring fused to a dibenzo structure. 3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one exhibits various biological activities and has potential applications in different fields.
Uses
Used in Pharmaceutical Industry:
3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one is used as a pharmaceutical agent for its potential therapeutic effects. It has been found to possess antioxidant, anti-inflammatory, and anticancer properties, making it a promising candidate for the development of new drugs to treat various diseases.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one is used as a dietary supplement due to its health-promoting properties. Its antioxidant and anti-inflammatory effects can contribute to overall wellness and help prevent chronic diseases.
Used in Cosmetic Industry:
3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one is used in the cosmetic industry as an active ingredient in skincare products. Its antioxidant properties can help protect the skin from environmental damage, while its anti-inflammatory effects may help reduce redness and irritation.
Used in Food Industry:
In the food industry, 3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one can be used as a natural preservative and antioxidant to extend the shelf life of food products and maintain their quality. Its potential health benefits also make it an attractive ingredient for functional foods and beverages.
Used in Agricultural Industry:
3,9-Dihydroxy-6H-dibenzo[b,d]pyran-6-one can be used in the agricultural industry as a natural pesticide or growth promoter. Its biological activities may help protect crops from pests and diseases, while also promoting healthy growth and yield.
Check Digit Verification of cas no
The CAS Registry Mumber 174023-48-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,0,2 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 174023-48:
(8*1)+(7*7)+(6*4)+(5*0)+(4*2)+(3*3)+(2*4)+(1*8)=114
114 % 10 = 4
So 174023-48-4 is a valid CAS Registry Number.
174023-48-4Relevant articles and documents
Scalable Multicomponent Synthesis of (Hetero)aryl-Substituted Phenyls: Focus on Metal-Free Halogenated Biaryls, 3-Arylindoles, and Isourolithine A Synthesis
Temperini, Andrea,Lanari, Daniela,Colognese, Francesco,Piazzolla, Francesca
, p. 7711 - 7719 (2019/12/12)
In the context of the growing interest of the scientific community for the development of sustainable synthetic strategies to access aromatic structures, we present a practical and metal-free approach to (hetero)biaryls which exploits the advantages of multicomponent reactions in sustainable solvents. In situ acid-catalysed generation of (hetero)aryl acetoxy dienes from the corresponding (hetero)arylidene acetones in a metal vessel, followed by Diels-Alder reaction using an electron-poor alkyne as dienophile, delivers the expected aromatic products after final oxidation of the cycloadduct. This protocol has been demonstrated as a convenient alternative to the previously reported synthetic strategies, considering its scalability and environmental sustainability and the low cost of substrates and equipment. Moreover, it has been successfully applied to the metal-free regioselective synthesis of (hetero)aryl-substituted-phenyls, 2-unsubstituted-3-aryl-indoles, and to the total synthesis of isourolithine A.
