Interesting facts
Interesting Facts about Ethyl 2-[1-(4-Chlorobenzoyl)-5-Methoxy-2-Methyl-Indol-3-Yl]Acetate
Ethyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate is an intriguing compound that merges synthetic chemistry with potential pharmacological applications. Here are some compelling aspects to consider:
- Indole Derivative: The presence of the indole structure in this compound is particularly noteworthy. Indoles are known for their role in a variety of biological processes and have been studied for their potential in medicinal chemistry.
- Substituent Effects: The introduction of the 4-chlorobenzoyl and methoxy groups significantly impacts the compound's chemical reactivity and biological activity. These substituents can enhance the interactions of the compound with biological targets.
- Potential Biological Activity: Compounds with indole rings, such as this one, have been researched for their role in drug development, particularly in the treatment of cancer and neurological disorders. The complexity of this molecule presents opportunities for further exploration in pharmacology.
- Synthetic Strategies: The synthesis of this compound likely involves multi-step reactions, demonstrating the creativity and problem-solving skills required in modern organic synthesis. Understanding the synthetic pathway can also provide insights into reaction mechanisms and functional group transformations.
- Structure-Activity Relationship: Investigating how changes in the structure of this compound affect its biological activity can be an enlightening endeavor. Medicinal chemists exploit these relationships to design more effective and selective drugs.
In summary, ethyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate is not just a chemical compound; it embodies the convergence of synthetic chemistry and biological potential. As a chemistry student or scientist, exploring this compound opens up pathways to understanding complex interactions within biological systems and contributions to pharmaceutical advancements.
Synonyms
Indomethacin ethyl ester
16401-99-3
8AON0U1UBT
1H-Indole-3-acetic acid, 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-, ethyl ester
DTXSID50167697
DTXCID4090188
Ethyl 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetate
Indomethacin ethyl
ethyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetate
CHEMBL328864
Ethyl [1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]acetate (Indomethacin Ethyl Ester)
BRN 0497742
1-(4-Chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetic acid ethyl ester; Indole-3-acetic acid, 1-(p-chlorobenzoyl)-5-methoxy-2-methyl-, ethyl ester (8CI); Ethyl 1-(4-chlorobenzoyl)-5-methoxy-2-methylindole-3-acetate; Ethyl 1-(p-chlorobenzoyl)-2-methyl-5-methoxy-3-indolylacetate; Indomethacin ethyl ester; Indometacin Impurity I
Indomethacin, ethyl ester
UNII-8AON0U1UBT
1-(p-Chlorobenzoyl)-5-methoxy-2-methyl-3-indoleacetic acid ethyl ester
Indometacin EP Impurity I
SCHEMBL4549122
COIRSVPTDJIIKY-UHFFFAOYSA-N
BDBM50090784
INDOLE-3-ACETIC ACID, 1-(p-CHLOROBENZOYL)-5-METHOXY-2-METHYL-, ETHYL ESTER
INDOMETACIN IMPURITY I [EP IMPURITY]
[1-(4-Chloro-benzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-acetic acid ethyl ester
Solubility of Ethyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate
Ethyl 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-indol-3-yl]acetate, a complex organic compound, presents interesting solubility characteristics worthy of exploration. This compound is likely to exhibit differential solubility based on a number of factors:
In summary, while specific solubility data for this compound may not be readily accessible, it can be expected to show variable solubility depending on the solvent type and environmental conditions. As is often the case with complex organic compounds, experimental determination is key to uncovering precise solubility behaviors.