CAS 216867-60-6
:[2,4'-Bipyridine]-5-carboxylicacid
Description:
[2,4'-Bipyridine]-5-carboxylic acid, with the CAS number 216867-60-6, is an organic compound characterized by its bipyridine structure, which consists of two pyridine rings connected by a carbon-carbon bond. The presence of a carboxylic acid functional group (-COOH) at the 5-position of one of the pyridine rings imparts acidic properties to the molecule. This compound is typically a white to off-white solid and is soluble in polar solvents such as water and alcohols, owing to the hydrophilic nature of the carboxylic acid group. It exhibits potential applications in coordination chemistry, particularly as a ligand in metal complexes, due to the nitrogen atoms in the pyridine rings that can coordinate with metal ions. Additionally, its structural features may contribute to biological activity, making it of interest in pharmaceutical research. The compound's stability and reactivity can be influenced by the presence of substituents on the pyridine rings, which can affect its electronic properties and interactions in various chemical environments.
Formula:C11H8N2O2
Synonyms:- 6-(2-Methoxypyrimidin-5-yl)-nicotinic acid
- 6-(Pyridin-4-yl)-nicotinic acid
- 6-(Pyrimidin-5-yl)-nicotinic acid
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Found 2 products.
[2,4'-Bipyridine]-5-carboxylic acid
CAS:<p>2,4'-Bipyridine-5-carboxylic acid is a chiral compound that has been synthesized by the solvothermal reaction of 2,4'-bipyridine and 5-carboxylic acid. The crystal structure is rhombic with a helical twist. The nitrate anion forms channels in the crystal structure, which allows for luminescence. This compound is also topologically similar to nicotinic acid, which is a known inhibitor of human nicotinic acetylcholine receptors (nAChRs). The framework also resembles that of nitrobenzene and other aromatic compounds.</p>Formula:C11H8N2O2Purity:Min. 95%Molecular weight:200.19 g/mol


