698359-01-2 Usage
Uses
Used in Organic Semiconductor Industry:
DIETHYL-BIS(BENZYLTHIO)TETRATHIAFULVALENE is used as an organic semiconductor material for its interesting electronic and conductive properties. Its unique structure allows for the manipulation of its electronic properties, making it a promising candidate for various applications in this industry.
Used in Organic Electronic Devices Development:
DIETHYL-BIS(BENZYLTHIO)TETRATHIAFULVALENE is utilized in the development of organic electronic devices due to its potential to enhance the performance and efficiency of these devices. Its electronic properties contribute to the improvement of device characteristics such as conductivity, stability, and energy efficiency.
Used in Synthesis of Functional Materials:
DIETHYL-BIS(BENZYLTHIO)TETRATHIAFULVALENE serves as a building block in the synthesis of functional materials. Its incorporation into the molecular structure of these materials can lead to the development of new materials with enhanced properties and applications in various fields, including electronics, energy storage, and sensing technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 698359-01-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,8,3,5 and 9 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 698359-01:
(8*6)+(7*9)+(6*8)+(5*3)+(4*5)+(3*9)+(2*0)+(1*1)=222
222 % 10 = 2
So 698359-01-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H24S6/c1-3-19-20(4-2)28-23(27-19)24-29-21(25-15-17-11-7-5-8-12-17)22(30-24)26-16-18-13-9-6-10-14-18/h5-14H,3-4,15-16H2,1-2H3
698359-01-2Relevant academic research and scientific papers
Hellberg, Jonas,Dahlstedt, Emma,Woldegiorgis, Andreas
, p. 1455 - 1463 (2004)
The 5-alkyl-2-dimethylamino-1,3-dithiolium-4-thiolate mesoion could be umpoled with sulfuryl chloride to yield a dicationic electrophile 3 that reacted with various electron-rich aromatic substrates to yield arylthio-substituted 1,3-dithiolium salts 13-25. Two of these compounds have been transformed to the corresponding symmetrical tetrathiafulvalenes 43 and 44, and their cyclovoltammetric behaviour recorded. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.
