63816-15-9 Usage
Description
2,2'-diselenobis[5-methoxyaniline] is an organic compound that integrates selenium and aniline components, known for its unique structural properties and functional groups containing selenium. 2,2'-diselenobis[5-methoxyaniline] is recognized for its potential in the development of new materials and has demonstrated significant utility in the realm of optoelectronics. Its capacity to act as an efficient catalyst in various chemical reactions and its intriguing characteristics make it a valuable subject for ongoing research and exploration of applications across different sectors of chemistry and materials science.
Uses
Used in Organic Synthesis:
2,2'-diselenobis[5-methoxyaniline] is utilized as a reagent in organic synthesis, leveraging its unique chemical properties to facilitate a range of reactions. Its presence can enhance the efficiency and selectivity of synthesis processes, making it a valuable component in the creation of complex organic molecules.
Used in Catalyst Development:
As an efficient catalyst, 2,2'-diselenobis[5-methoxyaniline] is employed to accelerate various chemical reactions. Its catalytic properties can be harnessed to improve reaction rates and yields, contributing to more sustainable and cost-effective chemical processes.
Used in Optoelectronics:
2,2'-diselenobis[5-methoxyaniline] is used as a material in the field of optoelectronics due to its light-sensitive properties. Its integration into devices can enhance performance in areas such as solar cells, light-emitting diodes (LEDs), and photodetectors, where its ability to interact with light is crucial.
Used in Materials Science:
In the realm of materials science, 2,2'-diselenobis[5-methoxyaniline] is used as a component in the development of new materials. Its unique structure and selenium-containing functional groups offer potential for creating materials with specialized properties, such as improved conductivity, stability, or sensitivity to environmental stimuli.
Used in Research and Development:
2,2'-diselenobis[5-methoxyaniline] is a subject of interest for research and development efforts aimed at uncovering new applications and enhancing existing ones. Its versatility and the intriguing properties associated with its selenium content make it a promising candidate for innovation in multiple chemical and material science domains.
Check Digit Verification of cas no
The CAS Registry Mumber 63816-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,8,1 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63816-15:
(7*6)+(6*3)+(5*8)+(4*1)+(3*6)+(2*1)+(1*5)=129
129 % 10 = 9
So 63816-15-9 is a valid CAS Registry Number.
63816-15-9Relevant articles and documents
Catalytic antioxidant activity of bis-aniline-derived diselenides as GPx mimics
Barbosa, Flavio A. R.,Bettanin, Luana,Botteselle, Giancarlo V.,Braga, Antonio L.,Canto, R?mulo F. S.,Ciancaleoni, Gianluca,Domingos, Josiel B.,Elias, Welman C.,Gallardo, Hugo,Rafique, Jamal,Saba, Sumbal,Salin, Drielly N. O.
, (2021/08/06)
Herein, we describe a simple and efficient route to access aniline-derived diselenides and evaluate their antioxidant/GPx-mimetic properties. The diselenides were obtained in good yields via ipso-substitution/reduction from the readily available 2-nitroaromatic halides (Cl, Br, I). These diselenides present GPx-mimetic properties, showing better antioxidant activity than the standard GPx-mimetic compounds, ebselen and diphenyl diselenide. DFT analysis demonstrated that the electronic properties of the substituents determine the charge delocalization and the partial charge on selenium, which correlate with the catalytic performances. The amino group concurs in the stabilization of the selenolate intermediate through a hydrogen bond with the selenium.
