59089-89-3

Usage

Uses

Used in Pharmaceutical Industry:
4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as a potential therapeutic agent for its antioxidant and neuroprotective effects, aiming to protect against oxidative stress and neurodegenerative diseases.
Used in Anti-Inflammatory Applications:
4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as an immunomodulatory agent to modulate inflammatory and immune responses in the body, potentially beneficial in treating inflammatory conditions.
Used in Cancer Research and Treatment:
4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as a potential anti-cancer agent, with research indicating its ability to target cancer cells and contribute to the development of novel cancer treatments.
Used in Diabetes and Obesity Research:
4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is used as a candidate for the development of drugs targeting diabetes and obesity, due to its potential anti-diabetic and anti-obesity effects, which could help in managing these conditions more effectively.

InChI:InChI=1/C5H4S5/c6-5-9-3-4(10-5)8-2-1-7-3/h1-2H2

Upstream product

• 75-15-0 carbon disulfide 
• 106-93-4 ethylene dibromide 

Downstream Products

• 55259-49-9 tetramethyltetraselenafulvalene 
• 66946-48-3 bis(ethylenedithio)tetrathiofulvalene 
• 101683-17-4 4',5'-dimethyl-4,5-(ethylenedithio)-1',3'-diselena-1,3-dithiafulvalene 
• 66946-49-4 bis(propylenedithio)tetrathiafulvalene 
• 74962-29-1 2,5,7,9-tetrathiabicyclo[4.3.0]non-1⁽⁶⁾-en-8-one 
• 216586-65-1 3-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiin-2-ylidene)-3H-isobenzofuran-1-one 
• 26393-26-0 tetrakis(trifluoromethyl)tetrathiafulvalene 
• 889764-29-8 C₁₀H₄F₆S₆ 
• 1246173-46-5 C₂₀H₁₂N₂O₄S₆ 
• 287924-79-2 5,6-bis-(tert-butyl-diphenyl-silanyloxymethyl)-5,6,5',6'-tetrahydro-[2,2']bi[[1,3]dithiolo[4,5-b][1,4]dithiinylidene] 
• 287924-74-7 5-(t-butyldiphenylsilyloxy)methyl-5,6-dihydro-2-(5',6'-dihydro-1,3-dithiolo[4,5-b]-1,4-dithiin-2'-ylidene)-1,3-dithiolo[4,5-b]-1,4-dithiin 

Relevant academic research and scientific papers

Thion- und Dithioester, XXIV Synthese von Tetrathiooxalestern

Reduction of carbon disulfide with potassium in dimethylformamide and subsequent alkylation yields the isotrithiones 2, which have been desulfurised with mercury acetate to give the 1,3-dithiol-2-ones 3. 2a is also available by a stepwise synthesis starting with methyl (methylthio)dithioacetate (6).The photochemical decarbonylation of 4,5-bis(methylthio)-1,3-dithiol-2-one (3a) leads to the formation of dimethyl tetrathiooxalate (11a).In solution 11a is in equilibrium with its dimer 13.Cyclic tetrathiooxalates are probably unstable at room temperature.