328933-58-0

Basic information

• Product Name: 4-{5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl}-phenol
• CAS NO: 328933-58-0
• Molecular Weight: 560.736
• Mol File: 328933-58-0.mol

Chemical Properties

• Boiling Point: 749.3±60.0 °C(Predicted)
• Density: 1.15±0.1 g/cm3(Predicted)
• CAS DataBase Reference: 4-{5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl}-phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-{5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl}-phenol(328933-58-0)
• EPA Substance Registry System: 4-{5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl}-phenol(328933-58-0)

Safety Data

• Hazardous Substances Data: 328933-58-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
4-5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl-phenol is used as a pharmaceutical compound for its potential therapeutic applications. 4-5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl-phenol's structural features may allow it to interact with specific biological targets, such as receptors or enzymes, which could be beneficial in the treatment of various diseases.
Used in Drug Delivery Systems:
In the field of drug delivery, 4-5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl-phenol may be utilized as a component in the design of novel drug delivery systems. Its unique structure could be exploited to enhance the solubility, stability, or targeted delivery of therapeutic agents, potentially improving their efficacy and reducing side effects.
Used in Chemical Research:
4-5-Benzyloxy-3-methyl-1-[4-(2-azepan-1-yl-ethoxy)-benzyl]-1H-indol-2-yl-phenol can also be used as a research tool in chemical and biological studies. Its synthesis and characterization can provide insights into the reactivity and properties of similar compounds, contributing to the development of new drugs and materials.

Relevant articles and documents

GLUCOPYRANOSIDES CONJUGATES OF 2-(4-HYDROXY-PHENYL)-1- 4-(2-AMIN-1-YL-ETHOXY)-BENZYL]-1H-INDOL-5-OLS

This invention provides tissue selective estrogens of formula (I) having structure (I) wherein: R1 and R2 are independently, hydrogen, alkyl chain of 1-6 carbon atoms, benzyl, acyl of 2-7 carbon atoms, benzoyl, (1) or (2); X is hydrogen, alkyl of 1-6 carbon atoms, CN, halogen, trifuoromethyl, or thioalkyl of 1-6 carbon atoms; n = 1-3; with the proviso that at least one of R1 or R2 is (1) or (2); or a pharmaceutically acceptable salt thereof.

Glucopyranosides conjugates of 2-(4-hydroxy-phenyl)-3-methyl-1-[4-(2-amin-1-yl-ethoxy)-benzyl]-1H-indol-5-ols

This invention provides tissue selective estrogens of formula I having the structure wherein: R1and R2are independently, hydrogen, alkyl chain of 1-6 carbon atoms, benzyl, acyl of 2-7 carbon atoms, benzoyl, X is hydrogen, alkyl of 1-6 carbon atoms, CN, halogen, trifluoromethyl, or thioalkyl of 1-6 carbon atoms; n=1-3; with the proviso that at least one of R1or R2are not hydrogen, alkyl chain of 1-6 carbon atoms, benzyl, acyl of 2-7 carbon atoms, or benzoyl; or a pharmaceutically acceptable salt thereof.