As a reactant to synthesize 3-(3,5-Dichlorophenyl)-2,4-oxazolidinedione (DCPO).[1]
To synthesize phenylcarbamate derivatives of cellulose and amylose, which are useful as polysaccharide-based chiral stationary phases (CSPs).{70][2][3]
Synthesis of regioselectively substituted cellulose derivatives and applications in chiral chromatography.
Acemoglu M, et al.
Chirality, 10(4), 294-306 (1998)
Nephrotoxic and hepatotoxic potential of imidazolidinedione-, oxazolidinedione-and thiazolidinedione-containing analogues of N-(3, 5-dichlorophenyl) succinimide (NDPS) in Fischer 344 rats.
Kennedy E, et al.
Toxicology, 186(1-2), 79-91 (2003)
Synthesis and chiral recognition of amylose derivatives bearing regioselective phenylcarbamate substituents at 2, 6-and 3-positions for high-performance liquid chromatography.
Shen J, et al.
Journal of Chromatography A, 1467, 199-205 (2016)
Polymer?bound cellulose phenylcarbamate derivatives as chiral stationary phases for enantioselective HPLC.
Ling F, et al.
Journal of Separation Science, 26(15?16), 1337-1346 (2003)
Toxicology in vitro : an international journal published in association with BIBRA, 29(7), 1887-1896 (2015-07-21)
Liver damage occurred in some patients who took troglitazone (TGZ) for type II diabetes. The 2,4-thiazolidinedione (TZD) ring in TGZ's structure has been implicated in its hepatotoxicity. To further examine the potential role of a TZD ring in toxicity we
Questions
Reviews
★★★★★ No rating value
Active Filters
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..