10374-80-8 Usage
Uses
Used in Optoelectronic Materials Production:
Dimethyl stilbene-4,4'-dicarboxylate is used as a key component in the manufacturing of optoelectronic materials due to its high thermal stability and resistance to UV radiation. Its properties contribute to the performance and durability of these materials in various applications.
Used in Organic Light-Emitting Diodes (OLEDs) Manufacturing:
Dimethyl stilbene-4,4'-dicarboxylate is utilized as a component in the production of OLEDs, where its light-harvesting and energy transfer capabilities enhance the efficiency and performance of these devices.
Used as a Fluorescent Sensor in Environmental Monitoring:
Dimethyl stilbene-4,4'-dicarboxylate serves as a fluorescent sensor for detecting various environmental pollutants, leveraging its light-harvesting properties to provide sensitive and selective detection methods.
Used in Photochemistry and Photophysics Research:
Dimethyl stilbene-4,4'-dicarboxylate has potential applications in the field of photochemistry and photophysics, where its ability to efficiently harvest light energy and transfer it to other molecules is of significant interest for advancing scientific understanding and developing new technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 10374-80-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,3,7 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 10374-80:
(7*1)+(6*0)+(5*3)+(4*7)+(3*4)+(2*8)+(1*0)=78
78 % 10 = 8
So 10374-80-8 is a valid CAS Registry Number.
10374-80-8Relevant academic research and scientific papers
Mechanochemical ruthenium-catalyzed olefin metathesis
Do, Jean-Louis,Mottillo, Cristina,Tan, Davin,trukil, Vjekoslav,Frii, Tomislav
supporting information, p. 2476 - 2479 (2015/03/04)
We describe the development of a mechanochemical approach for Ru-catalyzed olefin metathesis, including cross-metathesis and ring-closing metathesis. The method uses commercially available catalysts to achieve high-yielding, rapid, room-temperature metathesis of solid or liquid olefins on a multigram scale using either no or only a catalytic amount of a liquid.
