59089-89-3

Basic information

• Product Name: 4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE
• Synonyms: 5,6-DIHYDRO[1,3]DITHIOLO[4,5-B][1,4]DITHIINE-2-THIONE;4,5-ETHYLENEDITHIO-1,3-DITHIOL-2-THIONE;4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE;AKOS 92829;RARECHEM AR PA 0059;5,6-Dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-thione;Ethylenedithiodithiolethione;4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE 98+%
• CAS NO: 59089-89-3
• Molecular Formula: C₅H₄S₅
• Molecular Weight: 224.41
• Product Categories: Sulphur Derivatives;Charge Transfer Complexes (Synthetic Intermediates);Charge Transfer Complexes for Organic Metals;Functional Materials;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Others;S-Containing
• Mol File: 59089-89-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 123-126 °C(lit.)
• Boiling Point: 359°C at 760 mmHg
• Flash Point: 170.9°C
• Appearance: /
• Density: 1.74g/cm³
• Vapor Pressure: 5.05E-05mmHg at 25°C
• Refractive Index: 1.896
• CAS DataBase Reference: 4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE(59089-89-3)
• EPA Substance Registry System: 4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE(59089-89-3)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 59089-89-3(Hazardous Substances Data)

Usage

General Description

4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE is a chemical compound with potential pharmacological properties. It has been studied for its potential antioxidant and neuroprotective effects, as well as its ability to modulate inflammatory and immune responses in the body. Additionally, research indicates that 4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE may have potential anti-cancer properties and could be used in the development of novel cancer treatments. Furthermore, this compound has been found to possess potential anti-diabetic and anti-obesity effects, making it a promising candidate for the development of drugs targeting these conditions. Overall, 4,5-ETHYLENEDITHIO-1,3-DITHIOLE-2-THIONE shows promise in various biomedical applications and warrants further research to fully understand its potential benefits.

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

• 31366-25-3 tetrathiafulvalene 
• 66946-48-3 bis(ethylenedithio)tetrathiofulvalene 
• 97307-49-8 ethylenedithiotetrathiafulvalene 
• 55259-49-9 tetramethyltetraselenafulvalene 
• 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 
• 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] 

Relevant articles and documents

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.