3807-37-2 Usage
Uses
Used in Organic Synthesis:
2-(3-Thienylthio)thiophene is utilized as a key intermediate in organic synthesis for the creation of new molecules with potential biological activities. Its structural attributes facilitate the development of a diverse range of chemical compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(3-Thienylthio)thiophene serves as a valuable precursor for the synthesis of drugs. Its incorporation into molecular structures can lead to the discovery of novel therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Development:
2-(3-Thienylthio)thiophene is also employed in the design and synthesis of agrochemicals, where its unique properties can contribute to the creation of effective and environmentally friendly pesticides or herbicides.
Used in Optoelectronics:
2-(3-THIENYLTHIO)THIOPHENE has demonstrated potential in the optoelectronics field due to its interesting electronic and optical characteristics. It can be used as a component in the development of advanced materials for electronic devices, such as organic light-emitting diodes (OLEDs) and photovoltaic cells.
Used in Materials Science:
2-(3-Thienylthio)thiophene's properties make it a candidate for the advancement of materials with specific electronic, optical, or mechanical characteristics, contributing to innovations in various material science applications.
Check Digit Verification of cas no
The CAS Registry Mumber 3807-37-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,8,0 and 7 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 3807-37:
(6*3)+(5*8)+(4*0)+(3*7)+(2*3)+(1*7)=92
92 % 10 = 2
So 3807-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6S3/c1-2-8(10-4-1)11-7-3-5-9-6-7/h1-6H
3807-37-2Relevant academic research and scientific papers
Deryagina,Sukhomazova,Levanova
, p. 40 - 45 (2002)
The effect of methanol and ethanol on the route of the gas-phase reaction of 2-chlorothiophene with hydrogen sulfide, leading to 2-thiophenethiol and to bis(2-thienyl) sulfide, has been investigated. It was found that methanol significantly enhances this
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.
