242-51-3 Usage
Description
Dinaphtho[2,3-b:2',3'-d]furan, also known as DNBF, is a polycyclic aromatic hydrocarbon compound characterized by its unique fused ring structure. It is a yellow solid with a molecular formula of C24H14O, comprising two naphthalene rings fused to a furan ring. DNBF is recognized for its high thermal stability, fluorescence properties, and potential applications in various fields, including organic synthesis, analytical chemistry, optoelectronics, and organic electronics.
Uses
Used in Organic Synthesis:
Dinaphtho[2,3-b:2',3'-d]furan is used as a building block in the synthesis of organic compounds and materials, such as dyes, pigments, and pharmaceuticals. Its unique structure and properties make it a valuable component in the development of novel materials with desired characteristics.
Used in Analytical Chemistry:
DNBF serves as a reference standard for the identification and quantification of aromatic compounds. Its distinct properties allow for accurate analysis and detection of similar compounds in various samples.
Used in Optoelectronic Devices and Materials:
Leveraging its high thermal stability and fluorescence properties, Dinaphtho[2,3-b:2',3'-d]furan is utilized in the development of optoelectronic devices and materials. Its incorporation enhances the performance and efficiency of these devices, making it a sought-after component in this field.
Used in Organic Electronics:
Dinaphtho[2,3-b:2',3'-d]furan has been studied for its potential use in organic electronics, particularly in the fabrication of organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). Its properties contribute to improved device performance and open up new possibilities for the design and application of organic electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 242-51-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,4 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 242-51:
(5*2)+(4*4)+(3*2)+(2*5)+(1*1)=43
43 % 10 = 3
So 242-51-3 is a valid CAS Registry Number.
242-51-3Relevant articles and documents
Oxygen- and sulfur-bridged bianthracene V-shaped organic semiconductors
Mitsui, Chikahiko,Yamagishi, Masakazu,Shikata, Ryoji,Ishii, Hiroyuki,Matsushita, Takeshi,Nakahara, Katsumasa,Yano, Masafumi,Sato, Hiroyasu,Yamano, Akihito,Takeya, Jun,Okamoto, Toshihiro
, p. 931 - 938 (2017)
Highly π-electron conjugated backbones are of great interest for applications to organic electronic devices, e.g., organic field-effect transistors and organic photovoltaics. A series of oxygen- and sulfur-bridged bianthracene V-shaped π-electronic cores are facilely synthesized. Both V-shaped molecules possess bent structures induced by the intermolecular interaction in a herringbone-packing manner. A theoretical calculation study reveals that the driving force of the bent structures originates from the strong dispersion energy. Also, the bent conformation plays a vital role in the formation of a dense packing structure, resulting in an attractive intermolecular overlap. An examination of the charge transport demonstrates that the hole mobility is up to 2.0 sq cm/Vs. Sulfur-bridged V-shaped π-electronic cores are more suitable for two-dimensional carrier-transport than oxygen-bridged analogs.
