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PYRAZINE-2,3-DICARBOXYLICACIDIMIDE, commonly known as succinimide, is a crystalline compound with the molecular formula C6H4N2O3. It is derived from pyrazine and is widely recognized for its role as an intermediate in the synthesis of pharmaceuticals and agricultural chemicals. Succinimide's versatile chemical structure allows it to be a key component in various industrial applications, including the production of plastics, dyes, rubber compounds, and pesticides, as well as herbicides. Moreover, succinimide is under investigation for its potential medicinal properties, particularly in the treatment of neurodegenerative diseases and as an anticonvulsant. However, due to its potential hazards, it is crucial to exercise appropriate safety precautions when handling PYRAZINE-2,3-DICARBOXYLICACIDIMIDE.

4933-19-1

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4933-19-1 Usage

Uses

Used in Pharmaceutical Industry:
PYRAZINE-2,3-DICARBOXYLICACIDIMIDE is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its reactivity and structural properties to facilitate the creation of diverse medicinal compounds.
Used in Agricultural Chemical Industry:
Succinimide is utilized as a precursor in the production of agricultural chemicals, specifically pesticides and herbicides, where its chemical properties contribute to the effectiveness of these products in controlling pests and unwanted plant growth.
Used in Plastics Industry:
PYRAZINE-2,3-DICARBOXYLICACIDIMIDE is used as a precursor in the manufacturing of certain types of plastics, where its chemical structure plays a role in determining the plastic's properties, such as strength and flexibility.
Used in Dyes Industry:
Succinimide is employed in the production of dyes, where its chemical composition contributes to the color and stability of the dyes used in various applications, including textiles and printing.
Used in Rubber Industry:
PYRAZINE-2,3-DICARBOXYLICACIDIMIDE is used as a component in the formulation of rubber compounds, where it can influence the rubber's performance characteristics, such as elasticity and durability.
Used in Neurodegenerative Disease Treatment Research:
Succinimide is being studied for its potential use in the treatment of neurodegenerative diseases, where its medicinal properties are explored for their capacity to address or mitigate the symptoms and progression of these conditions.
Used in Anticonvulsant Medication Research:
PYRAZINE-2,3-DICARBOXYLICACIDIMIDE is also being investigated for its potential as an anticonvulsant, where its properties may contribute to the development of medications aimed at preventing or reducing the severity of seizures.

Check Digit Verification of cas no

The CAS Registry Mumber 4933-19-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,3 and 3 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4933-19:
(6*4)+(5*9)+(4*3)+(3*3)+(2*1)+(1*9)=101
101 % 10 = 1
So 4933-19-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3N3O2/c10-5-3-4(6(11)9-5)8-2-1-7-3/h1-2H,(H,9,10,11)

4933-19-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-Pyrazine dicarboxamide

1.2 Other means of identification

Product number -
Other names Pyrazin-dicarbonsaeure-imid

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:4933-19-1 SDS

4933-19-1Relevant articles and documents

PREPARATION AND STRUCTURAL ASSIGNMENTS OF SOME ISOMERIC 2,3-DISUBSTITUTED PYRIDINES

Spiessens, Luc I. M.,Anteunis, Marc J. O.

, p. 205 - 232 (2007/10/02)

The preparation of several isomeric 2,3-disubstituted pyridine compounds are described and their spectroscopical data given.IR and NMR spectra of quinolinimide, reported by Distefano et al., are contradicted.The electron impact mass spectra are found to be useful in the differentiation between positional isomers.

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