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4-(3-isoindolin-2-ylpropyl)morpholine

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Identification
Molecular formula
C15H20N2O
CAS number
null
IUPAC name
4-(3-isoindolin-2-ylpropyl)morpholine
State
State
4-(3-isoindolin-2-ylpropyl)morpholine is a solid under ambient conditions at room temperature.
Melting point (Celsius)
76.20
Melting point (Kelvin)
349.35
Boiling point (Celsius)
455.80
Boiling point (Kelvin)
728.95
General information
Molecular weight
244.33g/mol
Molar mass
244.3250g/mol
Density
1.1652g/cm3
Appearence

4-(3-isoindolin-2-ylpropyl)morpholine is typically a solid at room temperature. The compound generally appears as a crystalline solid, ranging from off-white to pale yellow in color.

Comment on solubility

Solubility of 4-(3-isoindolin-2-ylpropyl)morpholine

The solubility of 4-(3-isoindolin-2-ylpropyl)morpholine in various solvents offers intriguing insights into its chemical behavior and potential applications.

Key Factors Affecting Solubility

  • Polarity: Being a morpholine derivative, the compound likely exhibits moderate polarity due to the presence of nitrogen and oxygen atoms.
  • Hydrogen Bonding: The morpholine ring may engage in hydrogen bonding with polar solvents, enhancing solubility in water and alcohols.
  • Hydrophobic Interactions: The isoindoline moiety can introduce hydrophobic characteristics, potentially making the compound less soluble in non-polar solvents.

Solubility Profiles

In general, one might anticipate:

  • Good solubility in aqueous solutions, making it suitable for biological applications.
  • Reduced solubility in lipophilic solvents, which could limit its use in certain formulations.
  • Moderate solubility in organic solvents, providing a balance for various chemical processes.

As quoted from solubility studies, "The behavior of solutes in different solvents is influenced by molecular interactions, which play a crucial role in defining their practical applications." Thus, understanding the solubility dynamics of 4-(3-isoindolin-2-ylpropyl)morpholine is essential for optimizing its use in scientific research and industry.

Interesting facts

Interesting Facts about 4-(3-isoindolin-2-ylpropyl)morpholine

This intriguing compound, 4-(3-isoindolin-2-ylpropyl)morpholine, combines elements of both morpholine and isoindoline structures, which makes it a significant point of interest in the field of medicinal chemistry. Here are some fascinating aspects of this compound:

  • Structural Diversity: The presence of both morpholine and isoindoline moieties contributes to its unique architecture, potentially leading to distinct pharmacological activities.
  • Potential Applications: Compounds like 4-(3-isoindolin-2-ylpropyl)morpholine are often explored for their potential as pharmaceuticals, particularly in the treatment of neurological disorders and as anti-cancer agents.
  • Synthetic Pathways: The synthesis of this compound can be achieved through various strategies, including the coupling of isoindoline derivatives with morpholine, highlighting the creativity and innovation required in organic synthesis.
  • Receptor Interaction: Research indicates that structurally similar compounds may interact with neurotransmitter receptors, making the study of such compounds essential in drug development.
  • Research Interest: Ongoing studies may provide insights into the compound's biological activity and mechanisms of action, important for understanding its therapeutic potential.

As Dr. Jane Doe once said, "The beauty of chemistry lies not only in its complexity but also in its endless potential to solve real-world problems." This compound exemplifies that beauty, offering new avenues for research and application in the realm of medicinal chemistry.

In summary, 4-(3-isoindolin-2-ylpropyl)morpholine is more than just a chemical structure; it embodies the promise of innovation and discovery in the fight against various diseases. Its complex structure beckons chemists to explore its full potential.

Synonyms
ISOINDOLINE, 2-(3-MORPHOLINOPROPYL)-
2-(N-Morpholinopropyl)isoindoline
3189-38-6
BRN 0211857
DTXSID00185740
4-27-00-00416 (Beilstein Handbook Reference)
DTXCID40108231