CAS 124937-73-1
:2-Methoxy-5-methyl-γ-phenylbenzenepropanol
- 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:Formula:C17H20O2Purity:98%Color and Shape:SolidMolecular weight:256.3395Tolterodine EP Impurity A
CAS:Formula:C17H20O2Color and Shape:White To Off-White SolidMolecular weight:256.353-(2-Methoxy-5-methyl-phenyl)-3-phenyl-propan-1-ol
CAS:Formula:C17H20O2Purity:98%Color and Shape:SolidMolecular weight:256.3452-Methoxy-5-methyl-γ-phenylbenzenepropanol-d3
CAS:Controlled ProductApplications 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)Formula:C17H17D3O2Color and Shape:NeatMolecular weight:203.2362-Methoxy-5-methyl-γ-phenylbenzenepropanol
CAS:Controlled ProductImpurity 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)Formula:C17H20O2Color and Shape:NeatMolecular weight: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 incFormula:C17H20O2Purity:Min. 95%Molecular weight:256.34 g/mol






