62378-65-8 Usage
Uses
Used in Pharmaceutical Industry:
(E)-5,6-Dihydro-4-hydroxy-6-[2-(4-Methoxyphenyl)ethenyl]-2H-pyran-2-one is used as a pharmaceutical compound for its potential therapeutic applications. (E)-5,6-Dihydro-4-hydroxy-6-[2-(4-Methoxyphenyl)ethenyl]-2H-pyran-2-one's unique chemical structure allows it to interact with various biological targets, making it a promising candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (E)-5,6-Dihydro-4-hydroxy-6-[2-(4-Methoxyphenyl)ethenyl]-2H-pyran-2-one serves as a valuable compound for studying its chemical properties and potential reactions with other molecules. This can lead to the discovery of new chemical processes and the development of novel applications in various industries.
Used in Cosmetics Industry:
(E)-5,6-Dihydro-4-hydroxy-6-[2-(4-Methoxyphenyl)ethenyl]-2H-pyran-2-one may also find applications in the cosmetics industry due to its potential benefits for skin health and its ability to interact with biological molecules. It could be used as an active ingredient in skincare products, offering potential anti-aging, anti-inflammatory, or other beneficial effects.
Used in Flavor and Fragrance Industry:
Given its origin from Fijian kawa, (E)-5,6-Dihydro-4-hydroxy-6-[2-(4-Methoxyphenyl)ethenyl]-2H-pyran-2-one may have unique aromatic properties that could be utilized in the flavor and fragrance industry. It could be used to create new and distinct scents or flavors for various products, such as perfumes, candles, or even food and beverages.
Check Digit Verification of cas no
The CAS Registry Mumber 62378-65-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,7 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 62378-65:
(7*6)+(6*2)+(5*3)+(4*7)+(3*8)+(2*6)+(1*5)=138
138 % 10 = 8
So 62378-65-8 is a valid CAS Registry Number.
62378-65-8Relevant academic research and scientific papers
A rapid and diverse construction of 6-substituted-5,6-dihydro-4-hydroxy-2- pyrones through double Reformatsky reaction
Mineno, Masahiro,Sawai, Yasuhiro,Kanno, Kazuaki,Sawada, Naotaka,Mizufune, Hideya
, p. 10921 - 10926 (2014/01/06)
A rapid and diverse synthesis of biologically important 6-substituted-5,6-dihydro-4-hydroxy-2-pyrones through a double Reformatsky reaction of aldehydes to δ-hydroxy-β-ketoesters followed by lactonization is described. Due to the high functional group tolerance and reaction site discrimination between aldehyde, nitrile, and ester groups in the substrate, the protocol can provide the dihydropyrones with bromo, nitro, carboxylic acid, and β-ketoester groups, which are suitable for the further derivatizations. Furthermore, the protocol has been successfully applied to the rapid total synthesis of naturally occurring Yangonin.
