CAS 124937-73-1
:2-Metoxi-5-metil-γ-fenilbencenopropanol
- 2-Methoxy-5-methyl-γ-phenylbenzenepropanol
- 3-(2-Methoxy-5-Methylphenyl)-3-Phenylpropan-1-Ol
- 3-(2-Methoxy-5-methylphenyl)-3-phenylpropanol
- Benzenepropanol, 2-methoxy-5-methyl-γ-phenyl-
3-(2-Methoxy-5-Methylphenyl)-3-phenylpropan-1-ol
CAS:Fórmula:C17H20O2Pureza:96%Forma y color:SolidPeso molecular:256.3395Tolterodine EP Impurity A
CAS:Fórmula:C17H20O2Forma y color:White To Off-White SolidPeso molecular:256.353-(2-Methoxy-5-methyl-phenyl)-3-phenyl-propan-1-ol
CAS:Fórmula:C17H20O2Pureza:98%Forma y color:SolidPeso molecular:256.3452-Methoxy-5-methyl-γ-phenylbenzenepropanol-d3
CAS:Producto controladoApplications Isotope labelled 2-Methoxy-5-methyl-γ-phenylbenzenepropanol is a related compound to Tolterodine (T535795), a muscarinic receptor antagonist. Used in the treatment of urinary incontinence.
References Nilvebrant, L., et al.: Life Sci., 60, 1129 (1997), Nilvebrant, L., et al.: Eur. J. Pharmacol., 327, 195 (1997), Brynne, N., et al.: Int. J. Clin. Pharmacol. Ther., 35, 287 (1997)Fórmula:C17H17D3O2Forma y color:NeatPeso molecular:203.2362-Methoxy-5-methyl-γ-phenylbenzenepropanol
CAS:Producto controladoImpurity Tolterodine EP impurity A
Applications 2-Methoxy-5-methyl-γ-phenylbenzenepropanol is a related compound to Tolterodine (T535795), a muscarinic receptor antagonist. Used in the treatment of urinary incontinence.
References Nilvebrant, L., et al.: Life Sci., 60, 1129 (1997), Nilvebrant, L., et al.: Eur. J. Pharmacol., 327, 195 (1997), Brynne, N., et al.: Int. J. Clin. Pharmacol. Ther., 35, 287 (1997)Fórmula:C17H20O2Forma y color:NeatPeso molecular:256.342-Methoxy-5-methyl-gamma-phenylbenzenepropanol
CAS:2-Methoxy-5-methyl-gamma-phenylbenzenepropanol is a synthetic compound that is used as an intermediate in the synthesis of coumarin derivatives. Reaction with sulfonating agents produces sulfones, and reaction with borohydride reagents produces boronates. The synthesis of 2-methoxy-5-methyl-gamma-phenylbenzenepropanol can be accomplished by the reduction of diphenyl ethers with lithium aluminum hydride or borohydride. The reduction can also be carried out using lanthanum oxide and potassium borohydride. The reaction proceeds smoothly at room temperature in nonpolar solvents.
2-Methoxy-5-methyl-gamma-phenylbenzenepropanol reacts with chloride to produce the corresponding chlorides, which are useful intermediates for the synthesis of tolterodine tartrate, a drug used to treat urinary incFórmula:C17H20O2Pureza:Min. 95%Peso molecular:256.34 g/mol






