40316-76-5 Usage
Description
8-HYDROXY-7-METHOXYFLAVONE is a flavonoid-related compound characterized by its antioxidant properties. It is known for its potential role in the alleviation of diabetes mellitus and is derived from various plant sources.
Uses
Used in Pharmaceutical Applications:
8-HYDROXY-7-METHOXYFLAVONE is used as a therapeutic agent for the treatment of diabetes mellitus. Its antioxidant properties contribute to the mitigation of the disease's effects, providing a promising avenue for pharmaceutical research and development.
Used in Antioxidant Applications:
In the field of nutrition and health supplements, 8-HYDROXY-7-METHOXYFLAVONE is used as an antioxidant to combat oxidative stress and support overall health. Its ability to neutralize free radicals can contribute to the prevention of various diseases and the maintenance of cellular integrity.
Used in Nutraceutical Applications:
8-HYDROXY-7-METHOXYFLAVONE is also utilized in the nutraceutical industry as a natural ingredient with potential health benefits. It can be incorporated into dietary supplements and functional foods to enhance their antioxidant content and support the management of diabetes mellitus.
Check Digit Verification of cas no
The CAS Registry Mumber 40316-76-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,1 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40316-76:
(7*4)+(6*0)+(5*3)+(4*1)+(3*6)+(2*7)+(1*6)=85
85 % 10 = 5
So 40316-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H12O4/c1-19-13-8-7-11-12(17)9-14(20-16(11)15(13)18)10-5-3-2-4-6-10/h2-9,18H,1H3
40316-76-5Relevant articles and documents
A novel one-pot synthesis of flavones
Chang, Meng-Yang,Tsai, Min-Chen,Lin, Chun-Yi
, p. 11655 - 11662 (2021/03/31)
In this paper, a one-pot facile route for the BiCl3/RuCl3-mediated synthesis of functionalized flavones is described, including: (i) intermolecularortho-acylation of substituted phenols with cinnamoyl chlorides, and (ii) intramolecular cyclodehydrogenation of the resultingo-hydroxychalcones. The reaction conditions are discussed herein.
