Description
| Cat. No. | REF-B16006 |
| CAS. No. | 198480-21-6 |
| Molecular Formula | C44H46N2O3 |
| Molecular Weight | 650.86 g/mol |
| Synonyms | 1-[4-(2-AZEPAN-1-YL-ETHOXY)-BENZYL]-5-BENZYLOXY-2-(4-BENZYLOXY-PHENYL)-3-METHYL-1H-INDOLE; 1-[4-(2-AZEPAN-1-YL-ETHOXY)-BENZYL]-5-BENZYLOXY-2-(4-BENZYLOXY-PHENYL)-3-METHYL-1H-INDOLE; 1-[[4-[2-(azepan-1-yl)ethoxy]phenyl]methyl]-3-methyl-5-phenylmethoxy-2-(4-phenylmethoxyphenyl)indole; 5-Benzyloxy-2-(4-benzyloxy-phenyl)-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indole; 1-[[4-[2-(Hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3-methyl-5-(phenylmethoxy)-2-[4-(phenylmethoxy)phenyl]-1H-indole; BAZEDOXIFENE N-1; 1H-Indole, 1-[[4-[2-(hexahydro-1H-azepin-1-yl)ethoxy]phenyl]methyl]-3-methyl-5-(phenylmethoxy)-2-[4-(phenylmethoxy)phenyl]-; 1-(4-(2-(azepan-1-yl)ethoxy)benzyl)-5-(benzyloxy)-2-(4-(benz… |
| Purity | ≥98% |
| Appearance | Off-white to pale beige solid |
| Storage Temperature | 2-8°C |
| Applications | Bazedoxifene Impurity 7 can be useful in the preparation of N-alkyl indoles via Rh-catalyzed reactions of N-alkyl anilines with internal alkynes using the transient oxidizing directing group strategy. |
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