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Identification
Molecular formula
C22H29NO4
CAS number
.not available
IUPAC name
2-morpholinoethyl 2-(1-naphthylmethyl)-3-tetrahydrofuran-2-yl-propanoate
State
State

At room temperature, this compound is usually in a liquid state.

Melting point (Celsius)
10.30
Melting point (Kelvin)
283.50
Boiling point (Celsius)
343.20
Boiling point (Kelvin)
616.40
General information
Molecular weight
371.50g/mol
Molar mass
371.4970g/mol
Density
1.0903g/cm3
Appearence

This compound is typically a colorless to pale yellow liquid or oil.

Comment on solubility

Solubility of 2-Morpholinoethyl 2-(1-naphthylmethyl)-3-tetrahydrofuran-2-yl-propanoate

The solubility of 2-morpholinoethyl 2-(1-naphthylmethyl)-3-tetrahydrofuran-2-yl-propanoate is influenced by various factors due to its complex structure. This compound is likely to exhibit solubility characteristics typical of similar organic compounds.

Factors Affecting Solubility

  • Polarity: The presence of both hydrophilic (polar) and hydrophobic (non-polar) regions in the molecule may lead to varying solubility in different solvents.
  • Hydrogen Bonding: The morpholino group can form hydrogen bonds, which can enhance solubility in polar solvents such as water.
  • Alkyl Chains: The tetrahydrofuran and propanoate groups can affect the degree of solubility in organic solvents, favoring solubility in non-polar media.

Expected Solubility

Based on the aforementioned factors, the solubility of this compound may be categorized as:

  • Moderate in water, likely due to the presence of the morpholino moiety.
  • Good in organic solvents like ethanol or dichloromethane due to its hydrophobic components.

In conclusion, while precise solubility data is essential for practical applications, understanding the structural influences on solubility can provide valuable insights into the expected behavior of 2-morpholinoethyl 2-(1-naphthylmethyl)-3-tetrahydrofuran-2-yl-propanoate in various environments.

Interesting facts

Interesting Facts about 2-Morpholinoethyl 2-(1-Naphthylmethyl)-3-Tetrahydrofuran-2-Yl-Propanoate

2-Morpholinoethyl 2-(1-naphthylmethyl)-3-tetrahydrofuran-2-yl-propanoate is a fascinating compound used in various fields of chemistry and pharmacology. Here are several noteworthy aspects:

  • Structure: This compound features a unique morpholino ring, which contributes to its biological activity and solubility characteristics. The inclusion of a tetrahydrofuran ring adds to its structural complexity and overall stability.
  • Biological Significance: Compounds similar to this one have been explored for their potential therapeutic applications, particularly in the treatment of neurological disorders and as potential analgesics. Its structure suggests that it may interact with specific neurotransmitter systems.
  • Research Applications: As a derivative containing both a naphthyl group and a morpholine, this compound can serve as a valuable building block in medicinal chemistry to design more potent pharmaceutical agents. Researchers often investigate its derivatives for enhanced efficacy.
  • Interactions: The presence of the naphthyl group is particularly intriguing, as it might facilitate π-π stacking interactions with other aromatic systems, which can be critical for binding to biological targets.
  • Potential Synthesis Pathways: Chemists often explore various synthetic routes for such complex organic molecules, involving reactions such as nucleophilic substitutions and ring closure processes. Each synthetic pathway can significantly impact the yield and purity of the desired compound.

In summary, 2-morpholinoethyl 2-(1-naphthylmethyl)-3-tetrahydrofuran-2-yl-propanoate stands out due to its structural features and potential uses in drug design. As research continues, it may unveil even more applications and insights into its function!