17825-38-6 Usage
Description
2,4,5,7-tetramethylphenanthrene-9,10-dione, also known as rubiginone, is a naturally occurring chemical compound that belongs to the family of polycyclic aromatic hydrocarbons. It is found in certain species of fungi and lichens and is recognized for its unique chemical structure. This structure endows rubiginone with potential pharmacological and biological activities, such as antimicrobial and antiproliferative properties, making it a promising candidate for the development of new drugs and materials.
Uses
Used in Organic Chemistry:
Rubiginone is used as a building block in the field of organic chemistry for the synthesis of complex organic molecules. Its unique structure allows for versatile chemical modifications, facilitating the creation of novel compounds with potential applications in various industries.
Used in Pharmaceutical Development:
Rubiginone is used as a starting material for the development of new drugs due to its potential pharmacological activities. Its antimicrobial and antiproliferative properties make it a valuable compound for research into treatments for various diseases and conditions.
Used in Agricultural Applications:
Rubiginone has shown potential applications in agriculture, possibly serving as a natural pesticide or fungicide. Its antimicrobial properties could be harnessed to protect crops from harmful organisms, contributing to sustainable farming practices.
Used in Environmental Science:
In the field of environmental science, rubiginone's potential use in bioremediation or as an indicator of environmental contamination is being explored. Its presence in certain species of fungi and lichens may provide insights into ecological health and the impact of pollutants on natural ecosystems.
Each of these applications highlights the versatility and potential of 2,4,5,7-tetramethylphenanthrene-9,10-dione, or rubiginone, in contributing to advancements in chemistry, medicine, agriculture, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 17825-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,8,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 17825-38:
(7*1)+(6*7)+(5*8)+(4*2)+(3*5)+(2*3)+(1*8)=126
126 % 10 = 6
So 17825-38-6 is a valid CAS Registry Number.
17825-38-6Relevant articles and documents
Syntheses, Enrichment of Enantiomers, and Barriers to Racemization of Twisted 9,10-Phenanthrenquinones
Fritsch, Rainer,Hartmann, Erwin,Andert, Doris,Mannschreck, Albrecht
, p. 849 - 856 (2007/10/02)
The known syntheses of the 9,10-phenanthrenequinones 10a-c were improved by the chlorotrimethylsilane modification of the acyloin condensation of biaryl diesters.The novel quinones 4a, 4b, and 12 were prepared.For the first time, enantiomers (M and P) of this class of compounds were enriched semipreparatively by liquid chromatography on optically active sorbents.The barriers to thermal racemization amount to 90-130 kJ mol-1 (Table 2) and are thus higher than the barriers for the corresponding phenanthrene hydrocarbons by roughly 20 kJ mol -1.The reasons for this increase are discussed in terms of repulsive interactions in the trans ition state of helix inversion.
Sythesis of 2,2'-Diacyl-1,1'-biaryls. Regiocontrolled Protection of Ketones in Unsymmetrically Substituted 9,10-Phenanthrenequinones
Mervic, Miljenko,Ghera, Eugene
, p. 4720 - 4725 (2007/10/02)
A regiocontrolled monoketalization of unsymmetrically substituted phenanthrenequinones by use of 2,2-dimethyl-1,3-propanediol as the ketalizing reagent has been effected with the help of bromo substitution in one of the aromatic rings at the C-1 or C-8 po
