3593-75-7 Usage
Description
DITHIENO[2,3-B:2',3'-D]THIOPHENE (DTT) is a conductive material that serves as a donor building block for the synthesis of various optoelectronic materials. It is characterized by its yellow to red solid appearance and is known for its high charge mobility and environmental stability, making it a promising candidate for the development of organic electronic devices.
Uses
Used in Optoelectronic Applications:
DITHIENO[2,3-B:2',3'-D]THIOPHENE is used as an active layer for the development of organic electronic devices, such as organic thin film transistors, due to its high charge mobility and environmental stability.
Used in Electroluminescence Industry:
DITHIENO[2,3-B:2',3'-D]THIOPHENE is used as a key component in the creation of electroluminescent materials, which are essential for the development of advanced display technologies.
Used in Photochromism Applications:
DITHIENO[2,3-B:2',3'-D]THIOPHENE is utilized as a material for photochromic applications, where it can change its properties in response to light, enabling the development of smart materials and devices.
Used in Organic Photovoltaic (OPV) Solar Cells:
DITHIENO[2,3-B:2',3'-D]THIOPHENE is employed as a material in the fabrication of organic photovoltaic solar cells, contributing to their efficiency and performance in converting sunlight into electrical energy.
Check Digit Verification of cas no
The CAS Registry Mumber 3593-75-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3593-75:
(6*3)+(5*5)+(4*9)+(3*3)+(2*7)+(1*5)=107
107 % 10 = 7
So 3593-75-7 is a valid CAS Registry Number.
3593-75-7Relevant articles and documents
THERMAL HYDROTHIOLYSIS OF DI(2-THIENYL)SULFIDE IN THE GASEOUS AND LIQUID PHASE
Voronkov, M. G.,Deryagina, E. N.,Papernaya, L. K.,Sukhomazova, E. N.,Korchevin, N. A.,Efremova, G. G.
, p. 1301 - 1306 (2007/10/02)
At 500-600 deg C, di(2-thienyl)sulfide is converted to thiophene, thiophene thiols, dithienyls, and dithienothiophenes, and isomerized to 2,3-dithienylsulfide.Hydrogen sulfide accelerates these reactions significantly.In the liquid phase the thermal conversion of di(2-thienyl)sulfide takes place only with the participation of elemental sulfur or in the system sulfur-hydrogen sulfide.Thiophene and diethienothiophenes are not formed in this case, while isomerization occurs to a large degree.The observed thermal conversions of di(2-thienyl)sulfide are based on the addition of thiyl radicals to the double bonds of the thiophene ring and to the sulfide sulfur atom.
