40306-89-6 Usage
Uses
Used in Organic Electronic Devices:
[3,3'-Bithiophene]-2,2'-dicarboxaldehyde is used as a key component in the development of organic electronic devices, such as light-emitting diodes (OLEDs) and photovoltaic cells. Its unique molecular structure and electronic properties contribute to the enhancement of device performance and efficiency.
Used in Materials Science and Electronics:
[3,3'-Bithiophene]-2,2'-dicarboxaldehyde serves as a building block in the synthesis of other organic molecules with potential applications in materials science and electronics. Its versatility in molecular design allows for the creation of novel materials with tailored properties for various technological applications.
Used in Research and Development:
This bithiophene derivative is also utilized in research and development efforts aimed at discovering new organic semiconductor materials and advancing the field of organic electronics. Its strong electron-donating nature and electron transport capabilities make it an attractive candidate for further study and potential integration into innovative electronic and optoelectronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 40306-89-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,3,0 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 40306-89:
(7*4)+(6*0)+(5*3)+(4*0)+(3*6)+(2*8)+(1*9)=86
86 % 10 = 6
So 40306-89-6 is a valid CAS Registry Number.
40306-89-6Relevant academic research and scientific papers
Comparison of ullmann/RCM and ullmann/bis-hydrazone coupling reactions; New access to benzodithiophenes for dye-sensitized solar cell and thiahelicene applications
Stephenson, G. Richard,Cauteruccio, Silvia,Doulcet, Julien
, p. 701 - 707 (2014/04/03)
The use of CuTC (Liebeskind's catalyst), followed by methylenation and ring-closing metathesis, or bis-hydrazone coupling reactions is described. This approach establishes an alternative non-photochemical synthesis of the strategically important 1,2-b:4,3-b′ BDT regioisomer, which has previously been underused in applications such as dye-sensitized solar cells and nonlinear optics because of the difficulty of synthesis on a large scale. Georg Thieme Verlag Stuttgart. New York.
