124858-37-3 Usage
Description
5-Dehydroxyparatocarpin K is a flavonoid compound found in natural products such as plants and fruits. It exhibits a range of biological activities, including anti-inflammatory, antioxidant, and antimicrobial properties, and has potential applications in treating cancer and obesity.
Used in Pharmaceutical Industry:
5-Dehydroxyparatocarpin K is used as a therapeutic agent for its potential in treating various diseases and conditions, including cancer and obesity, due to its diverse range of biological activities.
Used in Cosmetic Industry:
5-Dehydroxyparatocarpin K is used as an active ingredient in skincare products for its anti-inflammatory and antioxidant properties, which can help protect and rejuvenate the skin.
Used in Food and Beverage Industry:
5-Dehydroxyparatocarpin K is used as a natural preservative and antioxidant in food and beverage products to extend shelf life and maintain freshness.
Used in Agricultural Industry:
5-Dehydroxyparatocarpin K is used as a natural antimicrobial agent in agriculture to protect crops from diseases and pests, promoting healthy growth and yield.
Note: The uses listed above are inferred from the provided materials and may not be exhaustive. Further research and development may reveal additional applications for 5-Dehydroxyparatocarpin K.
Check Digit Verification of cas no
The CAS Registry Mumber 124858-37-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,8,5 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 124858-37:
(8*1)+(7*2)+(6*4)+(5*8)+(4*5)+(3*8)+(2*3)+(1*7)=143
143 % 10 = 3
So 124858-37-3 is a valid CAS Registry Number.
124858-37-3Relevant articles and documents
New Syntheses of 4',7-Dihydroxy-6,8-di-C-prenylflavanone, Bavachin, Isobavachin and Related Compounds
Krishnamurti, M.,Parthasarathi, J.
, p. 247 - 248 (2007/10/02)
The titel compounds have been synthesised by nuclear prenylation of 4',7-dihydroxyflavanone(liquiritigenin, III), Cyclodehydrogenation of bavachin and isobavachin with DDQ yields the chromenoflavanones (VIII) and (X) respectively which on dehydrogenation
