2448-55-7

Usage

Uses

Used in Organic Synthesis:
1,4-Dithiin-2,3,5,6-tetracarbonitrile serves as a key intermediate in organic synthesis, particularly for the creation of complex organic molecules and pharmaceutical compounds. Its reactivity and structural features make it a valuable building block in the synthesis of a wide range of chemical products.
Used in Materials Science:
In the field of materials science, 1,4-Dithiin-2,3,5,6-tetracarbonitrile is used for the development of novel materials with electronic and optoelectronic properties. Its ability to form stable structures and complexes with other molecules contributes to the advancement of materials with specific electronic characteristics.
Used in Molecular Conductors and Semiconductors:
1,4-Dithiin-2,3,5,6-tetracarbonitrile is employed as a building block for the construction of molecular conductors and semiconductors. Its electron-donating and electron-accepting properties make it suitable for use in the design of materials with tailored electrical conductivity and semiconducting behavior.
Used in Pharmaceutical Research:
1,4-Dithiin-2,3,5,6-tetracarbonitrile has been investigated for its potential pharmacological activities, including antitumor and antimicrobial properties. The exploration of 1,4-Dithiin-2,3,5,6-tetracarbonitrile in drug discovery is driven by its unique chemical structure and the possibility of it interacting with biological targets to produce therapeutic effects.
Overall, 1,4-Dithiin-2,3,5,6-tetracarbonitrile is a versatile chemical compound with applications spanning across organic synthesis, materials science, molecular electronics, and pharmaceutical research, making it an important entity in the realm of chemical and material innovation.

Upstream product

• 75-15-0 carbon disulfide 
• 143-33-9 sodium cyanide 
• 773837-37-9 sodium cyanide 

Downstream Products

• 670-54-2 ethenetetracarbonitrile 
• 5927-80-0 bis(tetra-n-propylammonium) bis(2-mercapto-1,2-dicyanovinyl) sulfide 
• 75083-05-5 C₂₀H₁₄N₆O₂S₄ 
• 75083-06-6 [1,4]Dithiino[2,3-c;5,6-c']diisothiazole-3,7-dicarboxylic acid diphenyl ester 
• 75083-08-8 3,7-dibenzoyl-1,4-dithiino<2,3-c;6,5-c'>diisothiazole 
• 75111-90-9 2--4,5,6-tricyanothieno-<2,3-d>pyrimidine 
• 63419-92-1 N,N'-Bis(4-nitrophenyl)-N,N'-dimethyl-1,4-dithiino<2,3-c;6,5-c'>diisothiazol-3,7-dicarboxamid 
• 63419-93-2 N,N'-Bis(2-nitrophenyl)-N,N'dimethyl-1,4-dithiino-<2,3-c;6,5-c'>diisothiazol-3,7-dicarboxamid 
• 63419-89-6 N,N'-Bis(4-nitrophenyl)-1,4-dithiino<2,3-c;6,5-c'>diisothiazol-3,7-dicarboxamid 
• 63419-91-0 N,N'-Bis-(2-nitro-phenyl)-1,4-dithiino<2,3-c;6,5-c'>diisothiazol-3,7-dicarboxamid 
• 63419-88-5 N,N'-Bis(4-methoxyphenyl)-1,4-dithiino<2,3-c;6,5-c'>diisothiazol-3,7-dicarboxamid 
• 63419-87-4 1,4-Dithiino<2,3-c;6,5-c'>diisothiazol-3,7-dicarbonsaeure-dibenzylester 
• 63419-90-9 N,N'-Bis-(4-tolyl)-1,4-dithiino<2,3-c;6,5-c'>diisothiazol-3,7-dicarboxamid 
• 670-54-2 tetracyanoethylene anion 

Relevant academic research and scientific papers

The Tetracyanopyrrolide Anion as Ligand in Transition Metal Complexes

Two isotypic mononuclear discrete complexes [Co(MeCN)4(tcp) 2]·2MeCN (1) and [Ni(MeCN)4(tcp) 2]·2MeCN (2) containing the tetracyanopyrrolide anion [C 4(CN)4N]- (tcp) were synthes

Synthesis of functionalized tetracyanocyclopentadienides from tetracyanothiophene and sulfones

Tetracyanothiophene and tetracyano-1,4-dithiin react with a leaving group substituted carbon nucleophile such as ethyl benzenesulfonylacetate to afford substituted tetracyanocyclopentadienyl sodium derivatives in moderate to high yields through a putative condensation and desulfurization pathway. Subsequent functional-group transformation reactions on the Cp anion ring provided various C5R(CN)4- derivatives.

Structure and bonding of tetracyanopyrrolides

Salts bearing the tetracyanopyrrolide anion (TCP) were synthesized from tetracyano-1,4-dithiin and sodium azide according to a modified synthetic protocol. The solid-state structures of HTCP, MeTCP, Me4NTCP, NaTCP, and the ionic liquid EMIMTCP (EMIM = 1-ethyl-3-methylimidazolium) are discussed for the first time. According to experimental and computational data, the TCP anion can be regarded as a pseudohalide with π bonds highly delocalized over the entire anion including the four cyano groups. The planar anion is C 2v symmetric and represents a multifunctional binary CN ligand, which is capable of forming classic coordination bonds through the lone pairs of the CN groups or the ring nitrogen atom. In addition, noncovalent interactions such as π-π interactions are found and can be used to strengthen structural and electronic communication between organic ligands.

Decacyanooctatetraene Dianion: A Model System for Cyanocarbon-Based Conjugated Polymers

Decacyanooctatetraene (DCOT) has been prepared as its dianion and studied as a model compound for the prototypical n-dopable polymer poly(dicyanoacetylene) (PDCA).

Exploration of the pentacyano-cyclo-pentadienide ion, C5(CN) 5-, as a weakly coordinating anion and potential superacid conjugate base. Silylation and protonation

The reportedly unprotonatable pentacyano-cyclo-pentadienide ion, C 5(CN)5-, can be protonated and silylated at the cyano N atom using electrophilic reagents derived from weakly coordinating carborane anions.

Disproportionation of rosin in the presence of dithiin derivatives

Disclosed is a method of disproportionating rosin comprising heating said rosin in the presence of a dithiin derivative such, for example, as 2,5-diphenyl dithiin. The method can be carried out at about 150° C. to about 300° C. for about 1 hour to about 1