68160-34-9 Usage
Uses
Used in Organic Synthesis:
2,3-dimethoxy-5-[(4-methoxyphenyl)sulfanyl]cyclohexa-2,5-diene-1,4-dione is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3-dimethoxy-5-[(4-methoxyphenyl)sulfanyl]cyclohexa-2,5-diene-1,4-dione is employed as a starting material for the development of new pharmaceuticals. Its potential biological activities, such as antioxidant, anti-inflammatory, and antimicrobial properties, have been studied extensively. Researchers are exploring its use in the treatment of various diseases, including cancer, neurological disorders, and infectious diseases.
Used in Drug Discovery:
2,3-dimethoxy-5-[(4-methoxyphenyl)sulfanyl]cyclohexa-2,5-diene-1,4-dione is utilized in drug discovery as a lead compound for the identification of novel therapeutic agents. Its unique chemical structure and potential biological activities make it an attractive candidate for further optimization and development into effective drugs. Structure-activity relationship studies are conducted to modify its chemical properties and enhance its therapeutic potential.
Used in Chemical Research:
In the realm of chemical research, 2,3-dimethoxy-5-[(4-methoxyphenyl)sulfanyl]cyclohexa-2,5-diene-1,4-dione serves as a model compound for studying various chemical reactions and mechanisms. Its reactivity and selectivity in different reaction conditions provide valuable insights into the fundamental aspects of organic chemistry, contributing to the advancement of chemical knowledge and the development of new synthetic methodologies.
Used in Analytical Chemistry:
2,3-dimethoxy-5-[(4-methoxyphenyl)sulfanyl]cyclohexa-2,5-diene-1,4-dione is employed in analytical chemistry as a reference compound for the development and validation of analytical methods. Its unique chemical properties and stability make it suitable for the calibration of instruments and the assessment of method performance in various analytical techniques, such as chromatography, mass spectrometry, and spectrophotometry.
Check Digit Verification of cas no
The CAS Registry Mumber 68160-34-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,1,6 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 68160-34:
(7*6)+(6*8)+(5*1)+(4*6)+(3*0)+(2*3)+(1*4)=129
129 % 10 = 9
So 68160-34-9 is a valid CAS Registry Number.
68160-34-9Relevant academic research and scientific papers
Effect of Arylthiolated 2,3-Dimethoxy-1,4-benzoquinones on Respiratory Activity and Lipid Peroxidation in Bovine Heart Mitochondria
Mori, Koichi,Ushio, Tomoe,Okamoto, Tadashi,Kishi, Takeo,Sayo, Hiroteru
, p. 293 - 296 (2007/10/03)
A series of arylthiolated 2,3-dimethoxy-1,4-benzoquinones was synthesized and tested for the effect on the respiratory system and the lipid peroxidation in bovine heart mitochondria (BHM). These quinones showed intense inhibitory activities on the respiratory system in BHM. Their inhibitory activity in the succinate oxidase system was greater than that in the NADH oxidase system. No difference between the difference spectra, with and without these quinones, of the reduced minus oxidized forms of cytochromes (cyt.) suggested that these quinones inhibit at the site after cyt. a+a3 in the respiratory chain. Moreover, these quinones were as efficient as exogenous ubiquinone-10 (UQ-10) for the inhibition of lipid peroxidation. 5- And 5,6-di-arylthio groups on the quinone ring were found to be favorable for inhibition of the respiratory system and lipid peroxidation. Our results suggest that arylthiolated 2,3-dimethoxy-1,4-benzoquinones act as antioxidants by increasing the amount of endogenous reduced UQ-10 in BHM.
