26687-55-8 Usage
Explanation
Different sources of media describe the Explanation of 26687-55-8 differently. You can refer to the following data:
1. The compound's full name, which describes its structure and functional groups.
2. The compound belongs to the anthraquinone family, which is a group of organic compounds with a similar structure.
3. The compound's appearance, which is a yellowish-brown hue.
4. The compound does not dissolve in water but can dissolve in certain organic solvents, such as ethanol or methanol.
5. The compound is known for its antioxidant properties, which help protect cells from damage caused by free radicals. It also has potential anticancer properties, making it a subject of interest in the pharmaceutical and medical industries.
6. The compound is used in research and drug development due to its potential therapeutic benefits, particularly in the development of medications for various diseases.
7. The compound's properties make it a candidate for inclusion as an active ingredient in a range of medications, particularly those targeting cancer and other diseases.
8. The compound's unique properties and potential therapeutic benefits make it a popular choice for researchers and pharmaceutical companies working on new drug development.
Family
Anthraquinone
Color
Yellowish-brown
Solubility
Insoluble in water, soluble in organic solvents
Properties
Antioxidant and anticancer
Applications
Pharmaceutical and medical industries
Potential Active Ingredient
Various medications
Research and Drug Development
Commonly used
Check Digit Verification of cas no
The CAS Registry Mumber 26687-55-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,8 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26687-55:
(7*2)+(6*6)+(5*6)+(4*8)+(3*7)+(2*5)+(1*5)=148
148 % 10 = 8
So 26687-55-8 is a valid CAS Registry Number.
26687-55-8Relevant articles and documents
An efficient regioselective synthesis of endocrocin and structural related natural anthraquinones starting from emodin
Waser, Mario,Lackner, Bernd,Zuschrader, Joachim,Müller, Norbert,Falk, Heinz
, p. 2377 - 2380 (2005)
Endocrocin and related naturally occurring anthraquinone pigments like cinnalutein could be synthesized regioselectively via a Marschalk type reaction, starting from the natural hydroxy anthraquinone emodin. Furthermore, the new tri-O-methyl protected emodin-2-carbaldehyde may serve as a promising synthon for new bathochromically shifted, higher generation photodynamically active hypericin derivatives.
