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2,3-Pyrazinedicarboxylic acid
[CAS# 89-01-0]

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Identification
Classification Flavors and spices >> Synthetic spice >> Pyrazine fragrance
Name 2,3-Pyrazinedicarboxylic acid
Synonyms Pyrazine-2,3-dicarboxylic acid
Molecular Structure CAS # 89-01-0, 2,3-Pyrazinedicarboxylic acid, Pyrazine-2,3-dicarboxylic acid
Molecular Formula C6H4N2O4
Molecular Weight 168.11
CAS Registry Number 89-01-0
EC Number 201-875-3
SMILES C1=CN=C(C(=N1)C(=O)O)C(=O)O
Properties
Melting point 185-188 ºC
Water solubility soluble
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H315-H318-H335    Details
Precautionary Statements P261-P264-P264+P265-P271-P273-P280-P302+P352-P304+P340-P305+P354+P338-P317-P319-P321-P332+P317-P362+P364-P391-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Serious eye damageEye Dam.1H318
Eye irritationEye Irrit.2H319
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
2,3-Pyrazinedicarboxylic acid is a significant compound in the realm of organic chemistry and material science. It is a heterocyclic compound featuring a pyrazine ring with two carboxyl groups attached to the 2 and 3 positions. The presence of these carboxyl groups endows the molecule with unique chemical properties that have garnered interest for various applications.

The discovery of 2,3-pyrazinedicarboxylic acid emerged from efforts to explore the chemistry of pyrazine derivatives. Pyrazines are well-known for their ability to form stable structures and participate in diverse chemical reactions due to the presence of nitrogen atoms in the ring. The introduction of carboxyl groups at adjacent positions on the pyrazine ring enhances the molecule�s functionality by providing sites for further chemical modifications and interactions.

In pharmaceutical chemistry, 2,3-pyrazinedicarboxylic acid has shown potential as an intermediate in the synthesis of various bioactive compounds. The carboxyl groups facilitate the formation of esters and amides, which can be further modified to produce compounds with biological activity. Research has suggested that derivatives of 2,3-pyrazinedicarboxylic acid may exhibit significant pharmacological properties, including antimicrobial and anticancer activities.

The compound's applications extend into materials science as well. 2,3-Pyrazinedicarboxylic acid can be used as a precursor for the synthesis of advanced materials such as coordination polymers and metal-organic frameworks (MOFs). The carboxyl groups allow for the coordination with metal ions, leading to the formation of extended structures with potential uses in gas storage, catalysis, and sensing applications. The ability to form stable and well-defined frameworks makes it a valuable compound in the design of new materials with specific properties.

Additionally, 2,3-pyrazinedicarboxylic acid's role in organic synthesis is noteworthy. It can act as a building block for the creation of more complex molecules through reactions such as condensation and cyclization. This versatility in synthesis enhances its value as a key intermediate in the development of various chemical products.

Overall, 2,3-pyrazinedicarboxylic acid represents a versatile compound with significant implications in pharmaceuticals, materials science, and organic synthesis. Its unique chemical structure and functional groups provide a foundation for exploring new applications and advancing research in these fields.
Market Analysis Reports
List of Reports Available for 2,3-Pyrazinedicarboxylic acid
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