Interesting facts
Interesting Facts about 1,2,8-Trihydroxy-3-methoxy-6-methyl-anthracene-9,10-dione
This compound, known as an anthraquinone derivative, has garnered attention for several reasons in the field of chemistry and material science. Its unique structure serves as a fascinating platform for both academic research and practical applications.
- Biodiversity and Natural Sources: Compounds similar to this one can be found naturally in various plants, particularly in those with medicinal properties. For example, anthraquinones are often highlighted for their roles in the medicinal plants used traditionally in herbal medicine.
- Color Properties: Due to its chromophoric characteristics, the compound may exhibit significant color properties, ranging from vibrant shades to subtle hues. This quality makes it a candidate for dyes or pigments in various materials.
- Photochemical Activity: The presence of multiple hydroxyl groups in the structure enhances its reactivity, providing interesting avenues for photochemical studies. Compounds like this can absorb light energy and participate in complex photochemical reactions, useful for developing phototherapeutic applications.
- Electronics and Optoelectronics: Given its structural attributes, this compound may have potential applications in the fields of organic electronics and optoelectronics, contributing to the development of organic light-emitting diodes (OLEDs) and organic solar cells.
- Environmental Considerations: Its derivatives are often investigated for their roles in environmental chemistry. They can engage in redox reactions, offering insights into the biodegradation processes and the behavior of organic contaminants in ecosystems.
Research continues to explore the versatility of 1,2,8-trihydroxy-3-methoxy-6-methyl-anthracene-9,10-dione, particularly in understanding its reactivity, potential applications, and biological effects. This compound serves as a prime example of the intricate relationships between structure and function in the world of organic chemistry.
As we further delve into its properties, one cannot help but wonder, "What other secrets lie within the molecular architecture of anthraquinone derivatives?"
Synonyms
DERMOGLAUCIN
7213-59-4
Dermoglaucine
1,2,8-Trihydroxy-3-methoxy-6-methylanthraquinone
9L7A4MK3OC
Anthraquinone, 1,2,8-trihydroxy-3-methoxy-6-methyl-
9,10-Anthracenedione, 1,2,8-trihydroxy-3-methoxy-6-methyl-
ANTHRAQUINONE, 3-METHOXY-6-METHYL-1,2,8-TRIHYDROXY-
NSC-257448
Dermoglancin
1,2,8-trihydroxy-3-methoxy-6-methylanthracene-9,10-dione
NSC 257448
BRN 2480118
UNII-9L7A4MK3OC
SCHEMBL16226994
DTXSID10222438
NSC257448
DS-009122
9, 1,2,8-trihydroxy-3-methoxy-6-methyl-
Anthraquinone,2,8-trihydroxy-3-methoxy-6-methyl-
3-methyl-1,7,8-trihydroxy-6-methoxy-anthraquinone
6-Methoxy-3-methyl-1,7,8-trihydroxy-anthraquinone
TRIHYDROXY-3-METHOXY-6-METHYLANTHRAQUINONE, 1,2,8-
1,2,8-TRIHYDROXY-3-METHOXY-6-METHYL-9,10-ANTHRACENEDIONE
Solubility of 1,2,8-Trihydroxy-3-methoxy-6-methyl-anthracene-9,10-dione
The solubility of 1,2,8-trihydroxy-3-methoxy-6-methyl-anthracene-9,10-dione can be influenced by several factors, primarily due to its chemical structure. This compound features multiple hydroxyl groups that increase its potential for hydrogen bonding, which affects how it interacts with solvents.
Factors Affecting Solubility
In conclusion, while the solubility of 1,2,8-trihydroxy-3-methoxy-6-methyl-anthracene-9,10-dione is enhanced in polar solvents due to its multiple hydroxyl groups, it may exhibit reduced solubility in non-polar solvents. Understanding these dynamics is essential for its application in various chemical processes.