132018-13-4 Usage
Uses
Used in Pharmaceutical Industry:
6-Methoxy-3-(methoxycarbonyl)-2-(4-nitrophenyl)-4H-benzopyran-4-one is used as a synthetic intermediate for the production of flavonoids, which are known for their potential therapeutic applications, including antioxidant, anti-inflammatory, and anticancer properties.
Used in Cosmetic Industry:
In the cosmetic industry, 6-Methoxy-3-(methoxycarbonyl)-2-(4-nitrophenyl)-4H-benzopyran-4-one is used as a synthetic intermediate for the development of flavonoid-based skincare products, leveraging their antioxidant and anti-inflammatory properties to promote skin health and protect against environmental stressors.
Used in Nutraceutical Industry:
6-Methoxy-3-(methoxycarbonyl)-2-(4-nitrophenyl)-4H-benzopyran-4-one is utilized as a synthetic intermediate in the formulation of nutraceutical products containing flavonoids, which are believed to contribute to overall health and well-being by providing various health benefits, such as improved cardiovascular function and enhanced immune response.
Check Digit Verification of cas no
The CAS Registry Mumber 132018-13-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,1 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 132018-13:
(8*1)+(7*3)+(6*2)+(5*0)+(4*1)+(3*8)+(2*1)+(1*3)=74
74 % 10 = 4
So 132018-13-4 is a valid CAS Registry Number.
InChI:InChI=1/C18H13NO7/c1-24-12-7-8-14-13(9-12)16(20)15(18(21)25-2)17(26-14)10-3-5-11(6-4-10)19(22)23/h3-9H,1-2H3
132018-13-4Relevant academic research and scientific papers
Synthesis and Protein-Tyrosine Kinase Inhibitory Activities of Flavanoid Analogues
Cushman, Mark,Nagarathnam, Dhanapalan,Burg, Debra L.,Geahlen, Robert L.
, p. 798 - 806 (2007/10/02)
Treatment of o-hydroxyacetophenones 2a-e with excess lithium bis(trimethylsilyl)amide followed by dialkyl carbonates gave 3-(2-hydroxyaryl)-3-oxopropanoates 3a-e.The latter substances were transformed through the reaction of their magnesium chelates with
