64394-47-4

Basic information

• Product Name: BIS(CARBONYLDITHIO)TETRATHIAFULVALENE
• Synonyms: 2,2'-BIS(1,3,4,6-TETRATHIAPENTALENE-5-ONE);BIS(CARBONYLDITHIO)TETRATHIAFULVALENE;5-[5-Oxo[1,3]dithiolo[4,5-d]-1,3-dithiol-2-ylidene][1,3]dithiolo[4,5-d]-1,3-dithiol-2-one
• CAS NO: 64394-47-4
• Molecular Formula: C₈O₂S₈
• Molecular Weight: 384.6
• Product Categories: Charge Transfer Complexes (Synthetic Intermediates);Charge Transfer Complexes for Organic Metals;Functional Materials
• Mol File: 64394-47-4.mol
• Article Data: 4

Chemical Properties

• Melting Point: >360 °C
• Boiling Point: 534.017°C at 760 mmHg
• Flash Point: 244.097°C
• Appearance: /
• Density: 2.243g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 2.147
• CAS DataBase Reference: BIS(CARBONYLDITHIO)TETRATHIAFULVALENE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(CARBONYLDITHIO)TETRATHIAFULVALENE(64394-47-4)
• EPA Substance Registry System: BIS(CARBONYLDITHIO)TETRATHIAFULVALENE(64394-47-4)

Safety Data

• Hazardous Substances Data: 64394-47-4(Hazardous Substances Data)

Usage

General Description

BIS(CARBONYLDITHIO)TETRATHIAFULVALENE is a synthetic organic chemical compound that belongs to the family of tetrathiafulvalenes. It is commonly used as a ligand in coordination chemistry and as a building block for the synthesis of various organic compounds. The compound contains a tetrathiafulvalene core with two carbonyldithio groups attached to it, which gives it unique chemical properties and reactivity. BIS(CARBONYLDITHIO)TETRATHIAFULVALENE is known for its ability to form stable complexes with transition metal ions, making it useful in catalysis and materials science. It also has potential applications in organic electronics and molecular electronics due to its interesting electronic properties.

InChI:InChI=1/C8O2S8/c9-7-15-3-4(16-7)12-1(11-3)2-13-5-6(14-2)18-8(10)17-5

Upstream product

• 64394-45-2 2,5-diketo-1,3,4,6-tetrathiapentalene 
• 16005-62-2 bis-4,5-(trifluoromethyl)-1,3-dithiole-2-thione 
• 934-31-6 2-oxo-4,5-dicyano-1,3-dithiacyclopentene 

Downstream Products

• 66946-49-4 bis(propylenedithio)tetrathiafulvalene 
• 106920-29-0 tetrakis(pentylthio)tetrathiafulvalene 

Relevant articles and documents

ELECTROCHEMICAL REDUCTION OF CARBON DISULFIDE. SYNTHESIS OF CARBON SULFIDE HETEROCYCLES

Detailed procedures for the electrochemical reduction of carbon disulfide in N,N-dimethylformamide and acetonitrile are given.The synthetic utility of the method is demonstrated by the preparation of several thio-substituted derivatives of tetrathiafulvalene.Cyclic voltammograms of the tetrapotassium salt of the tetrathio anion of tetrathiofulvalene indicate four successive electron-transfer steps and in situ formation of a C6S8 species.Oxidation of the CS2 electrolysis solutions produces a compound which is tentatively identified as dithiolo-1,2,3-trithiole-5-thione.

Tetrathiapentalene and tetraselenapentalene compounds

This application is concerned with tetrathiapentalene and tetraselenapentalene compounds. Specifically, it is concerned with 1, 3, 4, 6-tetrathia-2, 5-dihetero-pentalene and 1, 3, 4, 6-tetraselena-2,5-dihetero-pentalene compounds having the formula STR1 w