Disodium pyridine-2,6-dicarboxylate

Base Information

• Chemical Name: Disodium pyridine-2,6-dicarboxylate
• CAS No.: 17956-40-0
• Molecular Formula: C7H5 N O4 . 2 Na
• Molecular Weight: 211.08256
• European Community (EC) Number: 241-882-9
• DSSTox Substance ID: DTXSID60170834
• Nikkaji Number: J260.805G
• ChEMBL ID: CHEMBL4521011
• Mol file: 17956-40-0.mol

Synonyms:Disodium pyridine-2,6-dicarboxylate;17956-40-0;EINECS 241-882-9;disodium;pyridine-2,6-dicarboxylate;2,6-Pyridinedicarboxylic acid, disodium salt;C7H5NO4.2Na;SCHEMBL3972222;C7-H5-N-O4.2Na;CHEMBL4521011;sodium 2,6-pyridinedicarboxylate;DTXSID60170834;AKOS028109533;2,6-Pyridinedicarboxylic acid disodium salt

Chemical Property of Disodium pyridine-2,6-dicarboxylate

Chemical Property:

• Vapor Pressure: 2.13E-09mmHg at 25°C
• Boiling Point: 463.7°Cat760mmHg
• Flash Point: 234.2°C
• PSA: 93.15000
• Density: g/cm³
• LogP: -2.19140
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 0
• Exact Mass: 210.98574614
• Heavy Atom Count: 14
• Complexity: 173

Purity/Quality:

98%Min ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=NC(=C1)C(=O)[O-])C(=O)[O-].[Na+].[Na+]

Refernces

Synthesis, single crystal structure and efficient catalysis for alcohol oxidation of a novel Ru(II) complex with both a N,N,N-tridentate ligand and a pyridinedicarboxylate

10.1016/j.poly.2015.08.047

The research focuses on the synthesis, characterization, and catalytic activity of a novel Ru(II) complex, Ru(pymieb)(pydic), for the oxidation of various alcohols. Key chemicals involved in this research include the newly synthesized N,N,N-tridentate ligand 2-(2-pyridylmethylamino)ethylbenzimidazole (pymaeb), disodium pyridine-2,6-dicarboxylate (pydic), and RuCl3, which are used to form the Ru(II) complex. The complex is characterized using NMR, FT-IR, HR-MS, and single crystal X-ray diffraction. The study demonstrates that this complex exhibits excellent catalytic activity for the oxidation of various alcohols to carbonyl compounds using tert-butyl hydroperoxide (TBHP) as the oxidant under mild and solvent-free conditions.

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