13063-09-7 Usage
Uses
Used in Pharmaceutical Industry:
2,4,6-Trimethoxycinnamic acid is used as a precursor in the synthesis of natural products and the development of new pharmaceuticals due to its potential biological and pharmacological properties.
Used in Antioxidant Applications:
2,4,6-Trimethoxycinnamic acid is used as an antioxidant agent for its ability to neutralize free radicals and protect cells from oxidative damage, which can contribute to various diseases and aging.
Used in Anti-inflammatory Applications:
2,4,6-Trimethoxycinnamic acid is used as an anti-inflammatory agent for its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Anticancer Applications:
2,4,6-Trimethoxycinnamic acid is used as a potential anticancer agent for its ability to inhibit the growth and proliferation of cancer cells, making it a promising candidate for further research and development in cancer treatment.
Used in Nutraceutical Industry:
2,4,6-Trimethoxycinnamic acid can be used as a functional ingredient in nutraceutical products for its health-promoting properties, such as antioxidant and anti-inflammatory effects, contributing to overall wellness and disease prevention.
Check Digit Verification of cas no
The CAS Registry Mumber 13063-09-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,6 and 3 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 13063-09:
(7*1)+(6*3)+(5*0)+(4*6)+(3*3)+(2*0)+(1*9)=67
67 % 10 = 7
So 13063-09-7 is a valid CAS Registry Number.
13063-09-7Relevant academic research and scientific papers
Radical-Cation Vinylcyclopropane Rearrangements by TiO2Photocatalysis
Maeta, Naoya,Kamiya, Hidehiro,Okada, Yohei
supporting information, p. 6551 - 6566 (2020/07/14)
Radical cation vinylcyclopropane rearrangements by TiO2 photocatalysis in lithium perchlorate/nitromethane solution are described. The reactions are triggered by oxidative single electron transfer, which is followed by immediate ring-opening of the cyclopropanes to generate distonic radical cations as unique reactive intermediates. This approach can also be applied to vinylcyclobutane, leading to the construction of six-membered rings. A stepwise mechanism via distonic radical cations is proposed based on preliminary mechanistic studies, which is supported by density functional theory calculations.
Palladium(II)-Catalyzed Oxidative Decarboxylative [2 + 2 + 1] Annulation of Cinnamic Acids with Alkynes: Access to Polysubstituted Pentafulvenes
Peng, Shiyong,Chen, Nuan,Zhang, Hong,He, Min,Li, Hongguang,Lang, Ming,Wang, Jian
supporting information, p. 5589 - 5593 (2020/07/08)
An unprecedented palladium(II)-catalyzed oxidative decarboxylative [2 + 2 + 1] annulation of cinnamic acids with alkynes has been developed for the synthesis of polysubstituted pentafulvenes. Ag2CO3 and DMSO are essential for the reaction. This protocol features readily available starting materials, a wide substrate scope, and moderate to excellent yields. Moreover, various significant frameworks can be easily obtained from the late-stage transformations of pentafulvenes via oxidation, reduction, and Scholl-type reaction.
