492-52-4 Usage
Uses
Used in Pharmaceutical Applications:
Hesperetin is utilized as a therapeutic agent for its potential anti-cancer properties, where it may inhibit the growth of cancer cells. It is also being studied for its capacity to reduce inflammation within the body, which can contribute to various health conditions.
Used in Cardiovascular Health:
Hesperetin is used as a dietary supplement to improve heart health and potentially lower the risk of cardiovascular diseases. Its antioxidant properties are believed to contribute to these benefits by protecting the heart from oxidative damage.
Used in Cosmetic and Skincare Industry:
In the cosmetic and skincare sector, Hesperetin is employed as an ingredient to enhance skin health and reduce the visible signs of aging. Its antioxidant capabilities are thought to protect the skin from environmental stressors and promote a more youthful appearance.
Used in Functional Foods and Beverages:
Hesperetin can be incorporated into functional foods and beverages as a natural antioxidant, capitalizing on its health-promoting properties to provide consumers with added nutritional benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 492-52-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,9 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 492-52:
(5*4)+(4*9)+(3*2)+(2*5)+(1*2)=74
74 % 10 = 4
So 492-52-4 is a valid CAS Registry Number.
InChI:InChI=1/C15H16O5/c1-7-4-9(16)13-11(19-7)6-10-8(14(13)17)5-12(20-10)15(2,3)18/h4,6,12,17-18H,5H2,1-3H3/t12-/m0/s1
492-52-4Relevant academic research and scientific papers
METHOD OF PRODUCING 4'-O-GLUCOSYL-5-O-METHYLVISAMMINOL
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Paragraph 0086, (2016/10/08)
PROBLEM TO BE SOLVED: To provide a chemical synthesis method for 4'-O-glucosyl-5-O-methylvisamminol used in a quality control test of Chinese medicine extract comprising Saposhnikovia roots. SOLUTION: According to a method of this invention, an acyl group is detached from a compound of a formula (2) (where R represents an acyl group) and an obtained diastereomer is separated to produce a compound of a formula (1). COPYRIGHT: (C)2015,JPOandINPIT