5629-55-0 Usage
Uses
Used in Textile Industry:
2,3,6,7-Tetramethoxyanthraquinone is used as a red dye for its ability to impart a vibrant color to fabrics, enhancing the visual appeal of textile products.
Used in Organic Electronic Devices:
2,3,6,7-Tetramethoxyanthraquinone is utilized as a semiconductor in the development of organic electronic devices, leveraging its electronic properties to improve device performance.
Used in Pharmaceutical Research:
2,3,6,7-Tetramethoxyanthraquinone is studied as a potential anti-cancer agent, with ongoing research exploring its ability to inhibit the growth of certain cancer cells.
Used in Anti-Inflammatory Research:
2,3,6,7-TETRAMETHOXYANTHRAQUINONE is also being investigated for its potential anti-inflammatory properties, which could be beneficial in the development of treatments for inflammatory conditions.
Used in Antimicrobial Research:
2,3,6,7-Tetramethoxyanthraquinone has been studied for its potential to inhibit the growth of certain bacteria and fungi, indicating its possible use in antimicrobial applications.
However, it is important to note that further research is required to fully understand the potential applications and safety profile of 2,3,6,7-Tetramethoxyanthraquinone in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 5629-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5629-55:
(6*5)+(5*6)+(4*2)+(3*9)+(2*5)+(1*5)=110
110 % 10 = 0
So 5629-55-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H16O6/c1-21-13-5-9-10(6-14(13)22-2)18(20)12-8-16(24-4)15(23-3)7-11(12)17(9)19/h5-8H,1-4H3
5629-55-0Relevant academic research and scientific papers
Studies on chromium trioxide-based oxidative coupling reagents and synthesis of lignan-cagayanone
Kuo,Lin
, p. 1507 - 1512 (2007/10/02)
Oxidation of 1-arylprop-1-enes by using the reagent system CrO3-HClO4- CH3CN at 0-5°C gave seven products from methyl isoeugenol, five from ethyl isoeugenol, four from benzyl isoeugenol, and five from isosafrole. Cagayanone was obtained from isosafrole in one step. The structures of the products were elucidated and the mechanism of their formation is discussed.
