3D-FM25981 - r-metoprolol
(R)-Metoprolol
CAS:Produto ControladoApplications (R)-Enantiomer of Metoprolol. Antihypertensive; antianginal; antiarrhythmic (class II).
References Johansson, et al.: Eur. J. Pharmacol., 24, 194 (1973), Luch, J.R., et al.: Anal. Profiles Drug Subs., 12, 325 (1983), Benfield, P., et al.: Drugs, 31, 376 (1986),Fórmula:C15H25NO3Cor e Forma:NeatPeso molecular:267.36(R)-Metoprolol-d7
CAS:Produto ControladoApplications Labelled (R)-enantiomer of Metoprolol. An antihypertensive, though up to 380 times less potent than the (S)-enantiomer.
References Toda, N., et al.: J. Pharm. Exp. Ther., 207, 311 (1978),Fórmula:C15H18D7NO3Cor e Forma:Light Yellow Solid With A Low Melting PointPeso molecular:274.411,2-Dihydroxy-3-isopropylaminopropane
CAS:Fórmula:C6H15NO2Pureza:98%Cor e Forma:LiquidPeso molecular:133.1888(2R)-1-[4-(2-methoxyethyl)phenoxy]-3-[(propan-2-yl)amino]propan-2-ol
CAS:Fórmula:C15H25NO3Pureza:95%Cor e Forma:LiquidPeso molecular:267.3639Metoprolol tartrate
CAS:Produto ControladoFórmula:C15H25NO3·C4H6O6Cor e Forma:NeatPeso molecular:684.81Metoprolol Tartrate
CAS:Produto ControladoFórmula:C15H25NO3·C4H6O6Cor e Forma:NeatPeso molecular:684.81alpha-Hydroxy Metoprolol (Mixture of Diastereomers)
CAS:Produto ControladoApplications A metabolite of Metoprolol.
References Lennard, M.S., et al.: Br. J. Clin. Pharmacol., 14, 713 (1982), Gengo, F.M., et al.: Clin. Pharmacol. Ther., 36, 320 (1984),Fórmula:C15H25NO4Cor e Forma:Off-White To BeigePeso molecular:283.36rac Metoprolol Hemi (+)-Tartrate
CAS:Produto ControladoApplications A β1 selective aryloxypropanolamine andrenergic antagonist which is used in the treatment of a variety of cardiovascular disorder (1,2).Antihypertensive; antianginal; antiarrhythmic (class II).
References 1. Johansson, B. et al.: Eur J Pharmacol. 1973 Nov;24(2):194-204.2. Benfield, P. et al.: Drugs. 1986 May;31(5):376-429.Fórmula:C15H25NO3·C4H6O6Cor e Forma:NeatPeso molecular:684.811,3-Bis[4-(2-methoxyethyl)phenoxy]-2-propanol
CAS:Produto ControladoApplications Metoprolol (M338790) impurity.
References Ruane, R., et al.: J. Pharm. Biomed. Anal., 8, 1091 (1990), Berger, T., et al.: J. Chromatogr. Sci., 29, 310 (1991),Fórmula:C21H28O5Cor e Forma:NeatPeso molecular:360.44rac 1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol
CAS:Produto ControladoImpurity Metoprolol USP Related Compound B
Applications An intermediate for the synthesis of β-chlorohydrins and β-chloroamines. An impurity found in metoprolol. Metroprolol USP Related Compound B.
References Moore, R., et al.: Marine Natural Products, 1, 43 (1978),Fórmula:C12H17ClO3Cor e Forma:ColourlessPeso molecular:244.713-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropane
CAS:Applications Impurity of Metoprolol.
References Lis, R., et al.: J. Med. Chem., 33(10), 2883 (1990)Fórmula:C12H16O3Cor e Forma:NeatPeso molecular:208.25(R)-3-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropane
CAS:Produto ControladoApplications Impurity of (R)-Metoprolol.
References Murthy, S., et al.: J. Labelled Comp. Radiopharm., 28, 1410 (1990),Fórmula:C12H16O3Cor e Forma:YellowPeso molecular:208.25(R)-(-)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride
CAS:(R)-(-)-alpha-Methoxy-alpha-trifluoromethyl-phenylacetyl chloride is an enantiomer that has a chiral center. It is used in the synthesis of metoprolol and bisoprolol, which are drugs that are prescribed to treat hypertension and angina pectoris. The racemate is used in the separation of amines by high performance liquid chromatography (Hplc). This compound also has a hydroxyl group and two fatty acids, which can be identified using a chromatographic method. The compound contains a chloride as well as a transfer group.Fórmula:C10H8ClF3O2Pureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:252.62 g/mol
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