CAS 6813-38-3
:2,2'-Bipyridyl-4,4'-dicarboxylic acid
Description:
2,2'-Bipyridyl-4,4'-dicarboxylic acid, with the CAS number 6813-38-3, is an organic compound characterized by its bipyridine structure, which consists of two pyridine rings connected by a carbon-carbon bond. This compound features two carboxylic acid groups (-COOH) located at the 4 and 4' positions of the bipyridine framework, contributing to its acidic properties and enhancing its solubility in polar solvents. It is typically a white to off-white crystalline solid and is known for its chelating ability, particularly with transition metals, making it useful in coordination chemistry and catalysis. The presence of the carboxylic acid groups allows for potential applications in organic synthesis, as well as in the development of metal-organic frameworks (MOFs) and other materials. Additionally, its structural features may impart interesting electronic and photophysical properties, making it a subject of interest in various fields, including materials science and medicinal chemistry.
Formula:C12H6N2O4
InChI:InChI=1/C12H8N2O4/c15-11(16)7-1-3-13-9(5-7)10-6-8(12(17)18)2-4-14-10/h1-6H,(H,15,16)(H,17,18)/p-2
SMILES:c1cnc(cc1C(=O)[O-])c1cc(ccn1)C(=O)[O-]
Synonyms:- Rarechem Al Be 0816
- 4,4'-Dicarboxy-2,2'-Bipyridine
- 2,2'-Biisonicotinic acid
- 2,2'-Dipyridyl-4,4'-Dicarboxylic acid
- 2,2'-Bipyridyl-4,4'-dicarboxyl
- 4,4'-Dicarboxylic Acid -2,2'-Dipyridine
- N'-(1-biphenyl-4-ylethenyl)-2-(3,4-dimethylphenoxy)acetohydrazide
- 2,2'-Bipyridine-4,4'-Dicarboxylate
- 2,2'-Bipyridine-4,4'-dicarboxylic acid
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Found 9 products.
2,2'-Bipyridine-4,4'-dicarboxylic Acid
CAS:Formula:C12H8N2O4Purity:>96.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:244.212,2'-Bipyridine-4,4'-dicarboxylic acid, 98%
CAS:<p>2,2'-Bipyridine-4,4'-dicarboxylic acid is used as an organic chemical synthesis intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar produc</p>Formula:C12H8N2O4Purity:98%Color and Shape:Crystals or powder or crystalline powder, White to cream or gray or pale pinkMolecular weight:244.214,4'-Dicarboxy-2,2'-bipyridine, 98%
CAS:<p>4,4'-Dicarboxy-2,2'-bipyridine, 98%</p>Formula:C12H8N2O4Purity:98%Color and Shape:white pwdr.Molecular weight:244.21[2,2'-Bipyridine]-4,4'-dicarboxylic acid
CAS:Formula:C12H8N2O4Purity:97%Color and Shape:SolidMolecular weight:244.20292,2'-Bipyridine-4,4'-dicarboxylic acid
CAS:<p>2,2'-Bipyridine-4,4'-dicarboxylic acid</p>Formula:C12H8N2O4Purity:≥95%Color and Shape: off-white to light yellow solidMolecular weight:244.20291g/mol2,2′-Dipyridyl-4,4′-dicarboxylic acid
CAS:Formula:C12H8N2O4Purity:97%Color and Shape:White to pale yellow crystalline powderMolecular weight:244.2062,2'-Bipyridine-4,4'-dicarboxylic acid
CAS:<p>2,2'-Bipyridine-4,4'-dicarboxylic acid (BBDA) is a synthetic molecule that has been used as an oxidant in organic synthesis. It is a redox-active compound with a reversible oxidation potential of +0.2 V. The electron transfer to the adjacent nitrogen atom is accompanied by light emission at 490 nm and chloride ion release. BBDA reacts with potassium dichromate in water to form 2,2'-bipyridine-6,6'-dicarboxylic acid and potassium chloride. This reaction can be monitored by magnetic resonance analysis and X-ray absorption spectroscopy. The formation of BBDA from dimethylformamide and esters has been reported in the literature.</p>Formula:C12H8N2O4Purity:Min. 95%Color and Shape:PowderMolecular weight:244.21 g/mol2,2'-Bipyridine-4,4'-dicarboxylic Acid
CAS:Controlled Product<p>Applications 2,2'-Bipyridine-4,4'-dicarboxylic acid<br></p>Formula:C12H8N2O4Color and Shape:NeatMolecular weight:244.2








