134589-26-7 Usage
Uses
Used in Organic Electronics Industry:
Anthracene, 2,3-bis(decyloxy)is utilized as a key component in the manufacturing of organic light-emitting diodes (OLEDs) for its ability to enhance the performance and efficiency of these devices. Its electron transporting properties are particularly beneficial in improving the overall functionality and longevity of OLEDs.
Used in Solar Cell Technology:
In the solar cell industry, Anthracene, 2,3-bis(decyloxy)serves as a valuable material due to its semiconducting nature, which is crucial for the conversion of light into electricity. Its electron transporting capabilities contribute to the efficiency of solar cells, making it a preferred choice for certain types of photovoltaic applications.
Used as a Chemical Intermediate:
Anthracene, 2,3-bis(decyloxy)also finds use as a chemical intermediate in the synthesis of various other organic compounds. Its unique structure allows for further chemical modifications and reactions, making it a versatile building block in organic chemistry for the development of new materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 134589-26-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,5,8 and 9 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 134589-26:
(8*1)+(7*3)+(6*4)+(5*5)+(4*8)+(3*9)+(2*2)+(1*6)=147
147 % 10 = 7
So 134589-26-7 is a valid CAS Registry Number.
134589-26-7Relevant academic research and scientific papers
Brotin, Thierry,Utermoehlen, Ralf,Fages, Frederic,Bouas-Laurent, Henri,Desvergne, Jean-Pierre
, p. 416 - 418 (1991)
2,3-Bis-n-decyloxyanthracene can form thermoreversible gels with alcohols at very low concentrations; electronic absorption spectra and fluorescence emission studies suggest that the network of the gel consists of head-to-tail assemblies of the aromatic component coexisting with the alcohol, the organization of the system essentially relying upon dipolar forces and van der Waals interactions.
Different synthetic routes towards efficient organogelators: 2,3-substituted anthracenes
Pozzo, Jean-Luc,Clavier, Gilles M.,Colomes, Michel,Bouas-Laurent, Henri
, p. 6377 - 6390 (2007/10/03)
Three synthetic approaches towards 2,3-substituted anthracenes are reported and discussed in terms of selectivity and viability. This allowed us to introduce a variety of substituents as sidearms. Promising results have been found using a tandem Diels-Alder aromatization reaction using 2,2,3-dimethoxybuladiene 9 as a key intermediate. However, for multigram preparations the Friedel-Crafts approach is preferred.
