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N-(3-morpholinopropyl)-2,2-diphenoxyacetamide

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Identification
Molecular formula
C20H24NO4
CAS number
132916-12-0
IUPAC name
N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide
State
State

At room temperature, it is generally found in a solid state, specifically a crystalline form. This attribute can affect both how it is stored and its potential uses in chemical reactions.

Melting point (Celsius)
94.50
Melting point (Kelvin)
367.65
Boiling point (Celsius)
548.20
Boiling point (Kelvin)
821.35
General information
Molecular weight
356.42g/mol
Molar mass
356.4220g/mol
Density
1.2120g/cm3
Appearence

The compound is typically a white to off-white crystalline solid. It can often appear either as a powder or crystalline solid form, which is common for many organic compounds used in a chemical synthesis context.

Comment on solubility

Solubility of N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide

N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide is a compound that presents interesting solubility characteristics. Understanding its solubility behavior is crucial for various applications, particularly in pharmaceuticals and chemical formulations. Here are some key aspects of its solubility:

  • Solvent Compatibility: This compound is generally soluble in organic solvents such as ethanol and DMSO due to its non-polar diphenoxy groups.
  • Water Solubility: Its solubility in water is expected to be low, largely influenced by the hydrophobic sections of the molecule. However, polar functional groups may enhance limited solubility.
  • Temperature Effects: Like many organic compounds, solubility may increase with temperature, allowing for greater dissolution in various solvents.
  • pH Dependency: The solubility in aqueous solutions can be altered by pH; changes may affect ionization of the amide functional group, impacting overall solubility.

In summary, while N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide may exhibit low water solubility, its compatibility with organic solvents makes it versatile for numerous applications. Further investigation and experimentation are typically required to assess specific solubility conditions for practical uses.

Interesting facts

Interesting Facts about N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide

N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide, often abbreviated for convenience, is an intriguing chemical compound that has garnered attention for various applications. Here are some notable facts:

  • Origin and Development: This compound is a synthetic derivative that incorporates morpholine, a heterocyclic compound. Morpholine has applications in pharmaceuticals and agrochemicals, highlighting the compound's relevance in medicinal chemistry.
  • Mechanism of Action: The unique structure of N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide suggests potential interactions with biological systems. Its diphenoxy motif may enhance lipophilicity, which is often key in facilitating drug permeability across cell membranes.
  • Pharmaceutical Potential: Research indicates that compounds containing morpholine often exhibit interesting biological activities. This compound may have therapeutic potential, particularly in areas such as anti-inflammatory and anti-cancer research.
  • Synthetic Versatility: The synthesis of this compound exemplifies creative organic chemistry techniques. Researchers may utilize various coupling reactions to merge the morpholinopropyl chain with the diphenoxy-acetamide portion, showcasing the adaptability of modern synthetic methodologies.
  • Potential for Research: With ongoing studies in medicinal chemistry and pharmacology, this compound serves as a promising candidate for exploring new therapeutic pathways. It represents an opportunity for further development, potentially leading to the discovery of novel drugs.

As we continue to evaluate the importance of chemical compounds like N-(3-morpholinopropyl)-2,2-diphenoxy-acetamide, it is evident that their unique structural features and potential applications in biological systems make them a point of interest in both academic and practical chemistry.