104515-79-9 Usage
Uses
Used in Organic Electronics:
2,3,6,7-Tetrakis(ethylthio)tetrathiafulvalene is used as a component in organic semiconductors for its electronic and redox properties, contributing to the development of advanced electronic devices.
Used in Materials Science:
In the field of materials science, 2,3,6,7-Tetrakis(ethylthio)tetrathiafulvalene is used as a building block for designing and synthesizing new materials with improved properties, such as enhanced conductivity and stability.
Used in Molecular Switches and Sensors:
2,3,6,7-Tetrakis(ethylthio)tetrathiafulvalene is used as a molecular switch and sensor due to its ability to undergo reversible redox reactions, which allows for the detection and response to specific stimuli.
Used in Energy Storage and Conversion Applications:
In the energy sector, 2,3,6,7-Tetrakis(ethylthio)tetrathiafulvalene and its derivatives are studied for their potential use in energy storage and conversion applications, such as batteries and solar cells, due to their unique structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 104515-79-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,1 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 104515-79:
(8*1)+(7*0)+(6*4)+(5*5)+(4*1)+(3*5)+(2*7)+(1*9)=99
99 % 10 = 9
So 104515-79-9 is a valid CAS Registry Number.
104515-79-9Relevant academic research and scientific papers
Yang, Xiaoguang,Rauchfuss, Thomas B.,Wilson, Scott
, p. 34 - 36 (1990)
Treatment of (Et4N)2 with SO2Cl2 gives molecular C6S10 (1), structurally characterized as (1)*(CS2)0.5, which has a channel structure; a two step conversion affords bicyclic tetrathiaindenone OC3S4*C2(CO2Me)2 which is used to make new alkenedithiolate derivatives.
New synthesis of phenyl-substituted 2,3-dihydro-1,3-dithiolo[4,5-e][1,4]dithiin-6-thione
Noh, Dong-Youn,Lee, Ha-Jin,Hong, Jongki,Underhill, Allan E.
, p. 7603 - 7606 (2007/10/03)
The facile synthesis of 4 and (±)-6 was carried out via a Diels-Alder type [2 + 4] cycloaddition reaction of oligomeric dien 8 with styrene or t-stilbene, respectively, as a dienophile by a thermal reaction and/or photoreaction (±)-6 crystallized as a rac
