2,3-Pyrazinedicarboxylic Acid
Catalog |
ACM89010 |
CAS |
89-01-0 |
Structure |  |
Synonyms |
3-Pyrazinedicarboxylic acid |
IUPAC Name |
Pyrazine-2,3-dicarboxylic acid |
Molecular Weight |
168.11 |
Molecular Formula |
C6H4N2O4 |
Canonical SMILES |
C1=CN=C(C(=N1)C(=O)O)C(=O)O |
InChI |
InChI=1S/C6H4N2O4/c9-5(10)3-4(6(11)12)8-2-1-7-3/h1-2H,(H,9,10)(H,11,12) |
InChI Key |
ZUCRGHABDDWQPY-UHFFFAOYSA-N |
Boiling Point |
297.01 °C |
Melting Point |
188 °C |
Purity |
95%+ |
Density |
1.6328 g/mL at 25 °C(lit.) |
Appearance |
White to Almost white powder to crystal |
Application |
2,3-Pyrazinedicarboxylic Acid serves multiple purposes, primarily recognized for its antifungal and antibacterial properties. It plays a crucial role as a reagent in the synthesis of transition metal pyrazinedicarboxylate complexes. The compound's anionic form has garnered significant interest in both coordination and supra-molecular chemistry due to its tendency to react with metal salts, producing insoluble polynuclear materials. This property extends its applications to crystal engineering, particularly in forming complexes with creatinine and 2-amino-4-hydroxy-6-methylpyrimidine. As a dicarboxylate ligand, 2,3-Pyrazinedicarboxylic Acid can link neighboring metal atoms to create one-dimensional chains in various complexes. Additionally, it demonstrates versatility by coordinating with neodymium(III) atoms in multiple bonding modes. When combined with neodymium nitrate, it facilitates the synthesis of coordination polymers with intricate three-dimensional frameworks through hydrothermal methods. |
Storage |
Store under inert gas |
Exact Mass |
168.01710661 |
Monoisotopic Mass |
168.01710661 |
Physical State |
Crystalline |
Refractive Index |
n20/D 1.4738(lit.) |
Storage Conditions |
Dry place,Room Temperature |
Topological Polar Surface Area |
100 Ų |
For Research Use Only. Not for use in diagnostic or therapeutic procedures.