CAS 139485-42-0
:2-Pyridinecarbonitrile, 3,4,5-trichloro-
Description:
2-Pyridinecarbonitrile, 3,4,5-trichloro- is a chemical compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. The presence of the cyano group (-C≡N) attached to the pyridine indicates its potential use in various chemical syntheses and applications. The compound is further modified by the presence of three chlorine atoms at the 3, 4, and 5 positions of the pyridine ring, which significantly influences its reactivity and physical properties. These chlorine substituents can enhance the compound's electrophilicity and may affect its solubility in organic solvents. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. Additionally, the presence of multiple halogen atoms often suggests potential applications in agrochemicals or materials science. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, 2-Pyridinecarbonitrile, 3,4,5-trichloro- is a versatile compound with significant implications in various fields of chemistry.
Formula:C6HCl3N2
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Found 2 products.
3,4,5-Trichloropicolinonitrile
CAS:<p>3,4,5-Trichloropicolinonitrile is a pyridine derivative that has been shown to be a potent inhibitor of the enzyme xanthine oxidase. Xanthine oxidase catalyses the oxidation of hypoxanthine to xanthine and then to uric acid. This reaction is important in the purification of nucleotides and in the production of uric acid as a component of urine. 3,4,5-Trichloropicolinonitrile binds reversibly to xanthine oxidase by means of its hydrazone group. It reacts with nucleophilic groups on the enzyme's surface and inhibits its activity by preventing access to substrates.<br>3,4,5-Trichloropicolinonitrile has been shown to inhibit xanthine oxidase from human erythrocytes and rat liver preparations.</p>Formula:C6HCl3N2Purity:Min. 95%Molecular weight:207.4 g/mol
