158871-27-3

Basic information

• Product Name: Propanenitrile, 3,3'-[[2-(5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-ylidene)-1,3-dithiole -4,5-diyl]bis(thio)]bis-
• CAS NO: 158871-27-3
• Molecular Formula: C14H12N2S8
• Molecular Weight: 464.791
• Mol File: 158871-27-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Propanenitrile, 3,3'-[[2-(5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-ylidene)-1,3-dithiole -4,5-diyl]bis(thio)]bis-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanenitrile, 3,3'-[[2-(5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-ylidene)-1,3-dithiole -4,5-diyl]bis(thio)]bis-(158871-27-3)
• EPA Substance Registry System: Propanenitrile, 3,3'-[[2-(5,6-dihydro-1,3-dithiolo[4,5-b][1,4]dithiin-2-ylidene)-1,3-dithiole -4,5-diyl]bis(thio)]bis-(158871-27-3)

Safety Data

• Hazardous Substances Data: 158871-27-3(Hazardous Substances Data)

Upstream product

• 74962-29-1 2,5,7,9-tetrathiabicyclo[4.3.0]non-1⁽⁶⁾-en-8-one 
• 158871-28-4 4,5-bis(2-cyanoethylthio)-1,3-dithiol-2-one 

Downstream Products

• 828938-09-6 [Sb(C₆H₅)(EDT-TTFS₂)] 
• 782500-50-9 [N-methylpyridinium][Au(triphenylphosphine)(2-((4,5-ethylenedithio)-1,3-dithiole-2-ylidene)-1,3-dithiole-4,5-dithionato)] 
• 782500-53-2 [Au₂(triphenylphosphine)2(2-((4,5-ethylenedithio)-1,3-dithiole-2-ylidene)-1,3-dithiole-4,5-dithionato)] 

Relevant articles and documents

Synthesis of New 2H-1,3-Dithiol-2-thiones and -2H-1,3-Dithiol-Ones, the Intermediates for Tetrathiafulvalenes and Metal Dithiolates

The synthesis of 2H-1,3-dithiol-2-thiones substituted in positions 4 and 5 was performed by the ring cleavage in 2,5,7,9-tetrathiobicyclonon-1(6)en-3-on-8-thione by sodium methoxide followed by alkylation of the obtained thiolate.The reactions of 2,4,5-tetrahydro-1,3-dithiol-2,4,5-trithione with cyclopentadiene, indene, diethylvinyldithiocarbamate, and allyl bromide, resulting new, earlier unaccessible, 2H-1,3-dithiol-2-thiones were carried out.Synthesis of new 2H-1,3-dithiol-3-thiones with substituents in 4 and 5 positions is performed; some of these compounds were transformed into related diketones by reacting with mercury acetate.New tetrathiofulvalenes are obtained.