
CAS 199191-66-7
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7 Produkte.
Duloxetine Related Compound H ((S)-4-{Methyl[3-(naphthalen-1-yloxy)-3-(thiophen-2-yl)propyl]amino}-4-oxobutanoic acid)
CAS:Nucleic acids and their salts, whether or not chemically defined; other heterocyclic compounds, nesoiFormel:C22H23NO4SFarbe und Form:White Crystalline PowderMolekulargewicht:397.13478Duloxetine USP Related Compound H
CAS:Formel:C22H23NO4SFarbe und Form:White To Off-White SolidMolekulargewicht:397.49(S)-Duloxetine Succinamide
CAS:Kontrolliertes Produkt<p>Impurity Duloxetine USP Related Compound H<br>Stability Hygroscopic<br>Applications An impurity of Duloxetine hydrochloride (D721000). It is formed by interaction of Duloxetine-HCl with enteric polymers. Duloxetine USP Related Compound H.<br>References Jansen, P.J., et al.: J. Pharmaceut. Sci., 87, 81 (1998),<br></p>Formel:C22H23NO4SFarbe und Form:NeatMolekulargewicht:397.49(S)-Duloxetine succinamide
CAS:Duloxetine succinamide is a chromatographic, solid, acidic compound. It has been synthesized by reacting (S)-duloxetine hydrochloride with succinic anhydride in the presence of triethylamine and acetonitrile. The reaction mixture was purified by high-performance liquid chromatography to produce the desired product. The purity of the compound was confirmed by postulating that it should have a reversed-phase HPLC profile similar to that of duloxetine succinate. Duloxetine succinamide is not soluble in water and is insoluble in organic solvents such as acetone, chloroform, ether, or benzene. The compound is stable at room temperature but decomposes when heated at higher temperatures. !--Formel:C22H23NO4SReinheit:Min. 95%Farbe und Form:PowderMolekulargewicht:397.49 g/mol(S)-Duloxetine-d7 Succinamide
CAS:Kontrolliertes Produkt<p>Applications A labelled impurity of Duloxetine hydrochloride (D721000). It is formed by interaction of Duloxetine-HCl with enteric polymers.<br>References Jansen, P.J., et al.: J. Pharmaceut. Sci., 87, 81 (1998),<br></p>Formel:C22D7H16NO4SFarbe und Form:NeatMolekulargewicht:404.531





