120120-58-3

Basic information

• Product Name: BEDO-TTF
• Synonyms: BIS(ETHYLENEDIOXY)TETRATHIAFULVALENE;BEDO-TTF;2-(5,6-dihydro-1,3-Dithiolo[4,5-b][1,4]dioxin-2-ylidene)-5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dioxin
• CAS NO: 120120-58-3
• Molecular Formula: C₁₀H₈O₄S₄
• Molecular Weight: 320.43
• Mol File: 120120-58-3.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 371℃
• Flash Point: 178℃
• Appearance: /
• Density: 1.78
• Vapor Pressure: 2.29E-05mmHg at 25°C
• Refractive Index: 1.814
• CAS DataBase Reference: BEDO-TTF(CAS DataBase Reference)
• NIST Chemistry Reference: BEDO-TTF(120120-58-3)
• EPA Substance Registry System: BEDO-TTF(120120-58-3)

Safety Data

• Hazardous Substances Data: 120120-58-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C10H8O4S4/c1-2-12-6-5(11-1)15-9(16-6)10-17-7-8(18-10)14-4-3-13-7/h1-4H2

Upstream product

• 934-36-1 2-thioxo-1,3-benzodithiole 
• 128347-04-6 2,5-dioxa-7,9-dithiabicyclo<4.3.0>non-1(6)-en-8-one 
• 35802-08-5 4,5-bis(methoxycarbonyl)-1,3-dithiole-2-one 
• 128457-00-1 4,5-ethylenedioxy-1,3-dithiole-2-thione 
• 88726-61-8 4,5-(vinylenedithio)-1,3-dithiole-2-one 
• 85720-62-3 1,3-dithiolo{4,5-d}-1,3-dithiol-2-one 
• 120120-62-9 5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dioxine-2-selone 
• 128346-57-6 5,6-dihydro-2-oxo-1,3-thiaselenolo[2,3-d][1,4]thiaselenin 
• 74962-30-4 2,6,8,10-Tetrathiabicyclo<5.3.0>dec-1(7)-en-9-on 
• 120120-61-8 4,5-ethylenedioxy-2-(N,N-dimethylamino)-1,3-dithiolium bromide 
• 120120-60-7 (3a-Bromo-tetrahydro-[1,3]dithiolo[4,5-b][1,4]dioxin-2-ylidene)-dimethyl-ammonium; bromide 
• 13855-85-1 2,3-bis(dimethyldithiocarbamyl)-1,4-dioxane 
• 120120-59-4 2-dimethyldithiocarbamyl-1,4-diox-2-ene 
• 844698-06-2 5,6-dimethoxy-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione 

Downstream Products

• 1421710-92-0 C₁₆H₁₆N₂O₄S₄*C₁₂H₄N₄ 

Relevant articles and documents

Efficient synthesis of EDO-S,S-DMEDT-TTF, a potent organic-donor for synthetic metals

Optically active ethylenedioxy-S,S-dimethylethylene-dithiotetrathiafulvalene (EDO-S,S-DMEDT-TTF: 1) has been synthesized in satisfactory yield using a triethyl phosphite-mediated cross-coupling of (5S,6S)-5,6-dimethyl-1,3-dithiolane-2-one 4 with unsubstituted 1,3-dithiolane-2-thione 6.

4,5-Ethylenedioxy-4',5'-ethylenedithiotetrathiafulvalene (EOET): a New Unsymmetrical Electron Donor

The synthesis, characterization, electrochemical properties, and preliminary X-ray structural data of the title electron donor, a hybrid of bis(ethylenedithio)tetrathiafulvalene and bis(ethylenedioxy)tetrathiafulvalene, are presented.

Anomalous ring cleavage of 1,3-dithiole- and 1,3-diselenole-2-thiones under the cross-coupling conditions using triethyl phosphite

The ring cleavage of 4,5-ethylenedioxy-1,3-dithiole- and -1,3-diselenole-2-thiones, followed by the reaction with 4,5- bis(methoxycarbonyl)-1,3-diselenole-2-one took place under the phosphite-mediated cross-coupling conditions to afford 2-thioxo- and 2-(s

Ethylenedithio(ethylenedioxo)diselenadithiafulvalene (TOST) and Ethylenediseleno(ethylenedioxo)tetrathiafulvalene (SO): New Unsymmetrical ?-Donors containing Three Elements in Group 16 (O, S, and Se)

The synthesis and characterization of new unsymmetrical bis(ethylenedithio)tetrathiafulvalene (ET) analogues ethylenedithio(ethylenedioxo)diselenadithiafulvalene (TOST) and ethylenediseleno(ethylenedioxo)tetrathiafulvalene (SO) that contain three elements in group 16 (O, S and Se) and their cation radical salts are reported.