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36023-64-0

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36023-64-0 Usage

General Description

1,4,5,6-Tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile is a chemical compound with the molecular formula C6H4N4O2. It is a pyrazine derivative that contains two oxo (carbonyl) groups and two cyano (carbonitrile) groups. 1,4,5,6-TETRAHYDRO-5,6-DIOXO-2,3-PYRAZINEDICARBONITRILE has potential applications in pharmaceuticals and materials science due to its unique chemical structure and properties. It is used as a building block in the synthesis of various organic compounds and can also be used as a starting material for the creation of novel drugs and materials. Additionally, it may have potential uses in the field of organic electronics and optoelectronics. However, further research is needed to fully explore the potential applications and properties of 1,4,5,6-Tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile.

Check Digit Verification of cas no

The CAS Registry Mumber 36023-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,2 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 36023-64:
(7*3)+(6*6)+(5*0)+(4*2)+(3*3)+(2*6)+(1*4)=90
90 % 10 = 0
So 36023-64-0 is a valid CAS Registry Number.

36023-64-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4,5,6-Tetrahydro-5,6-dioxo-2,3-pyrazinedicarbonitrile

1.2 Other means of identification

Product number -
Other names 2,3-Dicyano-1,4,5,6-tetrahydropyrazine-5,6-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36023-64-0 SDS

36023-64-0Relevant articles and documents

Cyclopentadienopyrazine organic compound and application thereof

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Paragraph 0149-0152, (2021/03/30)

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.

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

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Page/Page column 4, (2014/06/11)

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.

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

Morkved, Eva H.,Holmaas, Lars T.,Kjosen, Helge,Hvistendahl, Georg

, p. 1153 - 1156 (2007/10/03)

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.

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