65086-89-7 Usage
Uses
Used in Polymer and Resin Production:
Diphenyl [carbonylbis(imino-4,1-phenylenemethylene-4,1-phenylene)]biscarbamate is utilized as a crosslinking agent, which enhances the strength and stability of the resulting polymers and resins. Its ability to form robust crosslinks contributes to the improved mechanical properties and durability of these materials.
Used in Organic Electronics:
In the field of organic electronics, diphenyl [carbonylbis(imino-4,1-phenylenemethylene-4,1-phenylene)]biscarbamate is studied for its potential applications, likely due to its unique electronic properties and the possibility of integrating it into devices that require specific conductive or semiconductive characteristics.
Used in Optoelectronic Devices:
Diphenyl [carbonylbis(imino-4,1-phenylenemethylene-4,1-phenylene)]biscarbamate is also being investigated for its use in optoelectronic devices, where its complex structure and chemical properties may offer advantages in the development of components that interact with light, such as in solar cells, light-emitting diodes (LEDs), or photodetectors.
These applications highlight the versatility and importance of diphenyl [carbonylbis(imino-4,1-phenylenemethylene-4,1-phenylene)]biscarbamate in advancing material science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 65086-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65086-89:
(7*6)+(6*5)+(5*0)+(4*8)+(3*6)+(2*8)+(1*9)=147
147 % 10 = 7
So 65086-89-7 is a valid CAS Registry Number.
InChI:InChI=1/C41H34N4O5/c46-39(42-33-19-11-29(12-20-33)27-31-15-23-35(24-16-31)44-40(47)49-37-7-3-1-4-8-37)43-34-21-13-30(14-22-34)28-32-17-25-36(26-18-32)45-41(48)50-38-9-5-2-6-10-38/h1-26H,27-28H2,(H,44,47)(H,45,48)(H2,42,43,46)
65086-89-7Relevant academic research and scientific papers
Aresta, Michele,Dibenedetto, Angela,Quaranta, Eugenio
, p. 14145 - 14156 (1998)
In the presence of organophosphorus acids [Ph2P(O)OH, (PhO)2P(O)OH, (BuO)2P(O)OH, (BuO)P(O)(OH)2], aromatic diamines, such as 4,4'- methylendianiline (MDA) or 2,4-diaminotoluene (TDA), react with diphenylcarbonate (DPC) to afford in a very selective way mono- and dicarbamate phenyl esters. The carbamation process is strongly influenced by the temperature and solvent. The influence of both these factors on carbamate yield and selectivity has been investigated and we present in this study the kinetics of formation of both mono- and dicarbamate esters.
