4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholine
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- Molecular formula
- C15H18N2O2
- CAS Number
- 106261-48-7
- IUPAC Name
- 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholine
- Molecular Weight
- 272.33g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2400g/cm3
Identification
Interesting facts
Interesting Facts About 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholine
This compound, with its complex structure, is an intriguing member of the morpholine family known for its diverse applications in pharmaceutical science. Here are some fascinating aspects:
- Pharmaceutical Relevance: Compounds like 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholine are frequently researched for their potential therapeutic effects. Its derivatives have been explored in the treatment of various diseases, including certain cancers and neurological disorders.
- Structure-Activity Relationship (SAR): The presence of the isoxazole ring enhances the bioactivity of the molecule, making it a subject of interest in medicinal chemistry. The interaction between the morpholine and the isoxazole groups is critical for the compound’s pharmacological activity.
- Tuning Properties: Scientists can modify this compound to create analogues that could exhibit improved efficacy, reduced toxicity, or better bioavailability. Fine-tuning such structures often leads to breakthroughs in drug development.
- Role of the Phenyl Ring: The phenyl group attached to the isoxazole contributes to the lipophilicity of the molecule, which is essential for crossing biological membranes. This aspect plays a crucial role in drug design, affecting how the compound interacts with cellular targets.
In summary, the study of 4-[1-(3-phenylisoxazol-5-yl)ethyl]morpholine represents a compelling intersection of chemistry and medicine, showcasing how intricate molecular structures can lead to groundbreaking therapeutic advancements. As researchers continue to explore its potential, the value of understanding both its chemical makeup and biological implications cannot be overstated.