26314-39-6

Basic information

• Product Name: tetrakis(methoxycarbonyl)tetrathiafulvalene
• Synonyms: tetrakis(methoxycarbonyl)tetrathiafulvalene
• CAS NO: 26314-39-6
• Molecular Weight: 436.508
• Mol File: 26314-39-6.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: tetrakis(methoxycarbonyl)tetrathiafulvalene(CAS DataBase Reference)
• NIST Chemistry Reference: tetrakis(methoxycarbonyl)tetrathiafulvalene(26314-39-6)
• EPA Substance Registry System: tetrakis(methoxycarbonyl)tetrathiafulvalene(26314-39-6)

Safety Data

• Hazardous Substances Data: 26314-39-6(Hazardous Substances Data)

Upstream product

• 7396-41-0 4,5-bis(methoxycarbonyl)-1,3-dithiole-2-thione 
• 74962-30-4 2,6,8,10-Tetrathiabicyclo<5.3.0>dec-1(7)-en-9-on 
• 65259-97-4 4,5-propylenedithio-1,3-dithiole-2-thione 
• 35802-08-5 4,5-bis(methoxycarbonyl)-1,3-dithiole-2-one 
• 596814-99-2 4,7-bis(tert-butyldiphenylsilyloxy)-1,3-benzodithiole-2-thione 
• 77965-86-7 2-(α-nitrosobenzylidene)-4,5-bis-(methoxycarbonyl)-1,3-dithiole 
• 128457-00-1 4,5-ethylenedioxy-1,3-dithiole-2-thione 

Downstream Products

• 31366-25-3 tetrathiafulvalene 
• 51751-18-9 (Z)-[2,2']Bi[[1,3]dithiolylidene]-4,4'-dicarboxylic acid dimethyl ester 

Relevant articles and documents

New versatile building block for the construction of tetrathiafulvalene- based donor-acceptor systems

A new dissymmetrical tetrathiafulvalene (TTF) derivative 1 was synthesized as a versatile building block to reach TTF-based donor-acceptor assemblies incorporating C60 in triad C60-TTF-C60 2 and/or p-benzoquinone (Q) in fu

Unsymmetrically Substituted Ethylenedioxytetrathiafulvalenes

Seven new electron donors, 4,5-ethylenedioxytetrathiafulvalenes where 4',5'-substituents are trimethylenedithio, ethylenedithio, methylenedithio, 2-oxatrimethylenedithio, methylthio, hydrogen and methyl carboxylate, are prepared, and their electrochemical properties are investigated.

Some Novel Transformations of 1,4-Dithiafulvenes.

6-Phenyl-1,4-dithiafulvenes have been substituted at the 6-position by bromo, phenylazo, and nitroso groups; cation radical intermediates are proposed in these reactions.The 6-nitroso derivatives are deoxygenated by phosphines to give products derived from the fragmentation of intermediary nitrenes.