3D-FM25981 - r-metoprolol
(R)-Metoprolol
CAS:Prodotto controllatoApplications (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),Formula:C15H25NO3Colore e forma:NeatPeso molecolare:267.36(R)-Metoprolol-d7
CAS:Prodotto controllatoApplications 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),Formula:C15H18D7NO3Colore e forma:Light Yellow Solid With A Low Melting PointPeso molecolare:274.41Ref: ST-EA-CP-M17038
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CAS:Formula:C6H15NO2Purezza:98%Colore e forma:LiquidPeso molecolare:133.1888(2R)-1-[4-(2-methoxyethyl)phenoxy]-3-[(propan-2-yl)amino]propan-2-ol
CAS:Formula:C15H25NO3Purezza:95%Colore e forma:LiquidPeso molecolare:267.3639Metoprolol tartrate
CAS:Prodotto controllatoFormula:C15H25NO3·C4H6O6Colore e forma:NeatPeso molecolare:684.81Metoprolol Tartrate
CAS:Prodotto controllatoFormula:C15H25NO3·C4H6O6Colore e forma:NeatPeso molecolare:684.81alpha-Hydroxy Metoprolol (Mixture of Diastereomers)
CAS:Prodotto controllatoApplications 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),Formula:C15H25NO4Colore e forma:Off-White To BeigePeso molecolare:283.36rac Metoprolol Hemi (+)-Tartrate
CAS:Prodotto controllatoApplications 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.Formula:C15H25NO3·C4H6O6Colore e forma:NeatPeso molecolare:684.811,3-Bis[4-(2-methoxyethyl)phenoxy]-2-propanol
CAS:Prodotto controllatoApplications 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),Formula:C21H28O5Colore e forma:NeatPeso molecolare:360.44rac 1-Chloro-3-[4-(2-methoxyethyl)phenoxy]-2-propanol
CAS:Prodotto controllatoImpurity 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),Formula:C12H17ClO3Colore e forma:ColourlessPeso molecolare: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)Formula:C12H16O3Colore e forma:NeatPeso molecolare:208.25(R)-3-[4-(2-Methoxyethyl)phenoxy]-1,2-epoxypropane
CAS:Prodotto controllatoApplications Impurity of (R)-Metoprolol.
References Murthy, S., et al.: J. Labelled Comp. Radiopharm., 28, 1410 (1990),Formula:C12H16O3Colore e forma:YellowPeso molecolare: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.Formula:C10H8ClF3O2Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:252.62 g/mol
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