36023-64-0

Usage

Uses

Used in Pharmaceutical Industry:
1,4,5,6-TETRAHYDRO-5,6-DIOXO-2,3-PYRAZINEDICARBONITRILE is used as a building block in the synthesis of various organic compounds for its potential applications in the development of novel drugs. Its unique chemical structure allows for the creation of diverse pharmaceutical compounds with potential therapeutic effects.
Used in Materials Science:
1,4,5,6-TETRAHYDRO-5,6-DIOXO-2,3-PYRAZINEDICARBONITRILE serves as a starting material for the creation of new materials with specific properties. Its chemical structure can be utilized to develop materials with unique characteristics, such as high thermal stability, electrical conductivity, or optical properties, depending on the desired application.
Used in Organic Electronics:
1,4,5,6-TETRAHYDRO-5,6-DIOXO-2,3-PYRAZINEDICARBONITRILE may have potential uses in the field of organic electronics due to its electronic properties. Its incorporation into electronic devices, such as organic solar cells, organic light-emitting diodes (OLEDs), or organic field-effect transistors (OFETs), could enhance their performance and efficiency.
Used in Optoelectronics:
1,4,5,6-TETRAHYDRO-5,6-DIOXO-2,3-PYRAZINEDICARBONITRILE can be employed in optoelectronic applications, such as photodetectors, optical sensors, or optical communication systems, due to its potential optical properties. Its unique structure may contribute to the development of advanced optoelectronic devices with improved performance and sensitivity.
However, it is important to note that further research is required to fully explore the potential applications and properties of 1,4,5,6-Tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile, as its current uses are based on its chemical structure and potential, rather than proven applications.

Upstream product

• 79-37-8 oxalyl dichloride 
• 1187-42-4 diaminomaleonitrile 
• 18514-52-8 2,3-diaminomaleonitrile 

Downstream Products

• 56413-95-7 2,3-dichloro-5,6-dicyanopyrazine 
• 185827-54-7 5,6-Bis-benzylsulfanyl-pyrazine-2,3-dicarbonitrile 
• 112082-68-5 8-Benzyloxy-1,4,4b,9-tetraaza-fluorene-2,3-dicarbonitrile 
• 72545-77-8 C₁₂H₅Cl₂N₅ 
• 1379792-75-2 5-benzyl-6-phenyl-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitrile 
• 1379792-83-2 5-(benzylamino)-6-(phenylethynyl)pyrazine-2,3-dicarbonitrile 
• 1379792-76-3 5-(2-methoxyethyl)-6-phenyl-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitrile 
• 1379792-77-4 6-phenyl-5-(propan-2-yl)-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitrile 
• 1379792-78-5 5-(2-methylpropyl)-6-phenyl-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitrile 
• 1379792-79-6 6-phenyl-5-(tetrahydrofuran-2-ylmethyl)-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitrile 
• 1379792-80-9 5,6-diphenyl-5H-pyrrolo[2,3-b]pyrazine-2,3-dicarbonitrile 

Relevant academic research and scientific papers

Cyclopentadienopyrazine organic compound and application thereof

The invention relates to a cyclopentadienopyrazine organic compound and application thereof. The organic compound has a structure as shown in a general formula (1). The organic compound according to the present invention has excellent hole transport properties and stability, can be used as a hole injection layer material in an organic electroluminescent element, and can also be doped in a hole injection layer or a hole transport layer as a doping agent, so that a device can be driven at a low voltage, the electroluminescent efficiency can be improved, and the service life of the device can beprolonged.

Imidazopyrazine organic compound and application thereof

The invention relates to an imidazopyrazine organic compound and application thereof. The organic compound has a structure as shown in a general formula (1). The organic compound according to the present invention has excellent hole transport properties and stability, can be used as a hole injection layer material in an organic electroluminescent element, and can also be doped in a hole injectionlayer or a hole transport layer as a doping agent, so that a device can be driven at a low voltage, the electroluminescent efficiency can be improved, and the service life of the device can be prolonged.

Process for manufacturing bis(2-methoxyethyl)-2,3,6,7-tetracyano-1,4,5,8,9,10-hexazaanthracene

A process to manufacture substituted tetracyano-hexaazatricyclics with the substitutions occurring at the 9 and 10 hydrogens. The process begins with 2,3-dichloro-5,6-dicyanopyrazine, which is reacted to form the desired tetracyano-hexaazatricyclic. Different process embodiments enable different reaction paths to the desired tetracyano-hexaazatricyclic. Different tetracyano-hexaazatricyclic embodiments include bis(2-methoxyethyl)-2,3,6,7-tetracyano-1,4,5,8,9,10-hexazaanthracene and bis(2-methoxyethoxyethyl)-2,3,6,7-tetracyano-1,4,5,8,9,10-hexazaanthracene.

Highly efficient synthesis of 5,6-disubstituted-5H-pyrrolo[2,3-b]pyrazine- 2,3-dicarbonitriles through a one-pot palladium-catalyzed coupling reaction/cyclization in water

A highly efficient one-pot synthesis of 5,6-disubstituted-5H-pyrrolo[2,3-b] pyrazine-2,3-dicarbonitriles is presented. The reaction of 5-(alkyl-arylamino)- 6-chloropyrazine-2,3-dicarbonitriles with phenylacetylene, catalyzed by Pd-Cu, in the presence of SDS as the surfactant in water, leads to the desired products in good-to-high yields.

Preparation of magnesium azaphthalocyanines by cyclotetramerisation of S-substituted 4,5-disulfanylpyrazine-2,3-dicarbonitriles

Four novel S-substituted 4,5-disulfanylpyrazine-2,3-dicarbonitriles have been obtained in a multistep synthesis from diaminomaleonitrile. Two of these dicarbonitriles, with ethyl or benzyl S-substituents, give pure magnesium azaphthalocyanines in good yields when reacted with magnesium propoxide in propanol and dioxane. Aromatic S-substituents are less stable during the reaction conditions used for cyclisations, and product mixtures are obtained. Acta Chemica Scandinavica 1996.

Synthesis of Pyridoimidazopyrazines from 2,3-Dichloro-5,6-dicyanopyrazine with 2-Aminopyridines

Novel synthesis of the title compounds by the facile cyclization between 2,3-dichloro-5,6-dicyanopyrazine and various 2-aminopyridines under relatively mild conditions is described.The reactivity depended on the basicity of 2-aminopyridines.