3-Ethyl-2-methyl-5-(morpholinomethyl)-1,5,6,7-tetrahydroindol-4-one
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- Molecular formula
- C16H24N2O2
- CAS Number
- 40001-78-9
- IUPAC Name
- 3-ethyl-2-methyl-5-(morpholinomethyl)-1,5,6,7-tetrahydroindol-4-one
- Molecular Weight
- 274.37g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2057g/cm3
- Synonyms
- MOLINDONE
Identification
Interesting facts
Interesting Facts about 3-ethyl-2-methyl-5-(morpholinomethyl)-1,5,6,7-tetrahydroindol-4-one
3-ethyl-2-methyl-5-(morpholinomethyl)-1,5,6,7-tetrahydroindol-4-one is a fascinating compound that falls within the realm of indole derivatives, which are known for their diverse biological activities. Here are some noteworthy points about this compound:
- Pharmacological Potential: This compound has attracted attention for its potential therapeutic applications, particularly in the field of neuroscience and pharmaceuticals.
- Structural Diversity: The structure of this compound includes a morpholinomethyl group, which can enhance its solubility and bioavailability, making it a subject of interest for drug development.
- Indole Framework: The indole moiety is common in nature and serves as a backbone for many biologically active compounds, highlighting the significance of this class of molecules in medicinal chemistry.
- Derivatives Exploration: The unique combination of ethyl and methyl groups allows for the exploration of structure-activity relationships (SAR), which is crucial in optimizing the compound's efficacy.
- Research Interest: Studies have indicated that compounds with tetrahydroindole structures are often investigated for their effects on neurotransmitter systems, which could lead to advancements in treating mood disorders.
- Historical Context: The indole derivatives have a rich history in medicinal chemistry; for instance, many classic drugs such as tryptophan derived compounds have roots in this framework.
In summary, 3-ethyl-2-methyl-5-(morpholinomethyl)-1,5,6,7-tetrahydroindol-4-one is a compound that exemplifies the intricate relationship between chemical structure and biological activity, making it a pivotal topic for ongoing research and optimization in drug discovery.