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Phenacyl 2-morpholinoacetate

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Identification
Molecular formula
C15H17NO4
CAS number
None
IUPAC name
phenacyl 2-morpholinoacetate
State
State

At room temperature, Phenacyl 2-morpholinoacetate is in a solid state.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
320.00
Boiling point (Kelvin)
593.15
General information
Molecular weight
277.32g/mol
Molar mass
277.3160g/mol
Density
1.2100g/cm3
Appearence

Phenacyl 2-morpholinoacetate typically appears as a crystalline solid. Its color can range from off-white to light yellow, and it generally forms well-defined crystals.

Comment on solubility

Solubility of Phenacyl 2-morpholinoacetate

The solubility of phenacyl 2-morpholinoacetate can be quite interesting, as it is affected by a variety of factors. Generally, this compound demonstrates moderate solubility in polar solvents. Here are some key points to consider:

  • Polar Solvents: Phenacyl 2-morpholinoacetate is likely to dissolve well in solvents such as water and alcohols due to the presence of polar functional groups, which facilitate interactions through hydrogen bonding.
  • Non-Polar Solvents: Conversely, its solubility in non-polar solvents may be limited, as these environments do not promote effective solvation of the polar parts of the molecule.
  • pH Sensitivity: The solubility may also be influenced by pH levels, especially if there are ionizable groups present, leading to variations when adjusting the acidity or alkalinity of the solution.
  • Temperature Dependence: Increasing temperature typically enhances solubility for most solids, therefore changing the temperature can result in significant differences in solubility behavior.

In summary, the solubility of phenacyl 2-morpholinoacetate can be described as:

  1. Moderate in polar solvents
  2. Poor in non-polar solvents
  3. Variable with changes in pH and temperature

Understanding these solubility characteristics is crucial for applications in various chemical processes and formulations.

Interesting facts

Interesting Facts about Phenacyl 2-Morpholinoacetate

Phenacyl 2-morpholinoacetate is a compound that showcases the fascinating intersection of organic chemistry and pharmacology. Here are some compelling insights about this intriguing compound:

  • Origin of the Name: The name phenacyl derives from "phenacetin," a well-known analgesic, along with a reference to its morpholinoacetate structure, hinting at its possible biological significance.
  • Biological Activity: This compound is often studied for its potential therapeutic effects. It is believed to have properties that may be beneficial in medicinal chemistry, particularly in drug development.
  • Role of Morpholino Group: The morpholino component of the compound contributes significantly to its properties. Morpholines are known for their ability to enhance solubility and permeability in biological systems, making them valuable in pharmaceuticals.
  • Synthesis: Phenacyl 2-morpholinoacetate can be synthesized through various organic reactions. Understanding these synthesis pathways is essential for identifying ways to create more effective analogs in pharmaceutical research.
  • Research Applications: Currently, researchers are exploring the application of this compound in numerous studies related to cancer treatment and other diseases due to its potential mechanisms of action.

In conclusion, phenacyl 2-morpholinoacetate exemplifies the importance of understanding chemical compounds not just in isolation but within the broader context of medicinal chemistry and pharmacology. As scientists continue to uncover the nuances of such compounds, we gain invaluable insights into their potential therapeutic benefits.

Synonyms
MOBECARB
15518-84-0
phenacyl 2-morpholin-4-ylacetate
Mobecarbe
Mobecarbo
Mobecarb [INN]
Phenacyl 4-morpholineacetate
46LG9K0Y24
Mobecarbum
Mobecarbo [INN-Spanish]
Mobecarbe [INN-French]
Mobecarbum [INN-Latin]
UNII-46LG9K0Y24
EINECS 239-551-9
SCHEMBL2108130
CHEMBL2106776
DTXSID40165849
WIELTBTVQBNULW-UHFFFAOYSA-N
NS00025040
4-Morphineacetic acid, phenylcarbonylmethyl ester
Q27258944