CAS 90770-88-0
:4,4'-Dihydroxy-2,2'-bipyridine
Description:
4,4'-Dihydroxy-2,2'-bipyridine, with the CAS number 90770-88-0, is an organic compound characterized by its bipyridine structure, which consists of two pyridine rings connected by a carbon-carbon bond. This compound features hydroxyl (-OH) groups at the 4 and 4' positions of the bipyridine framework, contributing to its solubility in polar solvents and enhancing its potential for hydrogen bonding. It typically appears as a solid at room temperature and may exhibit a range of colors depending on its purity and form. The presence of hydroxyl groups also suggests that it may participate in various chemical reactions, including oxidation and complexation with metal ions, making it of interest in coordination chemistry and materials science. Additionally, its structural features may impart specific biological activities, although detailed studies would be necessary to elucidate any such properties. Overall, 4,4'-Dihydroxy-2,2'-bipyridine is a versatile compound with potential applications in various fields, including organic synthesis and catalysis.
Formula:C10H8N2O2
Synonyms:- [2,2'-Bipyridine]-4,4'-diol
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Found 4 products.
4,4'-DIHYDROXY-2,2'-BIPYRIDINE
CAS:Formula:C10H8N2O2Purity:98%Color and Shape:SolidMolecular weight:188.18274,4'-Dihydroxy-2,2'-bipyridine
CAS:4,4'-Dihydroxy-2,2'-bipyridinePurity:97%Molecular weight:188.18g/mol4,4'-Dihydroxy-2,2'-bipyridine
CAS:<p>4,4'-Dihydroxy-2,2'-bipyridine is a metallo-organic compound that can be used as a homogeneous catalyst for the oxidation of hydroxyl groups. It is also used in cancer research because it has been shown to inhibit tumor cell proliferation and induce apoptosis. 4,4'-Dihydroxy-2,2'-bipyridine is an activated form of 2,2'-bipyridyl with a hydroxyl group on its ortho position. It can be prepared by reacting bromine with the metal salt of 2-hydroxybenzaldehyde in the presence of sodium hydroxide. This reaction produces two products: 4,4'-dihydroxy-2,2'-bipyridine and 2-bromoethanol. The deuterium isotope is used for nuclear magnetic resonance spectroscopy studies because it has a spin quantum number of one and does not cause chemical shift</p>Formula:C10H8N2O2Purity:Min. 98 Area-%Color and Shape:White PowderMolecular weight:188.18 g/mol1H,1’H,4H,4’H-[2,2′-bipyridine]-4,4′-dione
CAS:Purity:98%Color and Shape:SolidMolecular weight:188.1860046



