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5-Methyl-6-phenylmorpholin-3-one

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Identification
Molecular formula
C11H13NO2
CAS number
: 38360-95-7
IUPAC name
5-methyl-6-phenyl-morpholin-3-one
State
State

In its pure form, 5-Methyl-6-phenylmorpholin-3-one is a solid at room temperature, typically in crystalline form. It remains stable under standard conditions of temperature and pressure.

Melting point (Celsius)
74.00
Melting point (Kelvin)
347.15
Boiling point (Celsius)
293.50
Boiling point (Kelvin)
566.60
General information
Molecular weight
205.24g/mol
Molar mass
205.2630g/mol
Density
1.1627g/cm3
Appearence

5-Methyl-6-phenylmorpholin-3-one is a solid compound. It is typically characterized by its crystalline form which is common among similar morpholinone derivatives. The compound may appear colorless to pale yellow depending on purity and specific conditions of synthesis.

Comment on solubility

Solubility of 5-Methyl-6-phenyl-morpholin-3-one

The solubility of 5-methyl-6-phenyl-morpholin-3-one can vary based on several factors including temperature and the solvent used. Here are key points to consider:

  • Polar solvents: This compound tends to dissolve better in polar solvents due to its morpholine ring structure, which contains polar bonds.
  • Non-polar solvents: Solubility in non-polar solvents may be limited because the presence of the phenyl group creates regions of hydrophobicity.
  • Temperature effects: Generally, an increase in temperature will enhance the solubility of many compounds, including potentially this one, as kinetic energy allows for better interaction with the solvent.
  • pH dependency: The solubility may be influenced by the pH of the solution; variations can lead to protonation or deprotonation of functional groups, thereby altering solubility characteristics.

However, it is critical to conduct experimental solubility tests in specific conditions to determine the exact solubility profile of 5-methyl-6-phenyl-morpholin-3-one. This compound's behavior in different environments can provide important insights into its practical applications and effectiveness in chemical formulations.

Interesting facts

Interesting Facts about 5-Methyl-6-phenyl-morpholin-3-one

5-Methyl-6-phenyl-morpholin-3-one is an intriguing compound that stands out for its unique structure and potential applications. Here are some fascinating insights into this compound:

  • Structure: The compound features a morpholine ring, a six-membered ring containing nitrogen and oxygen. This structural element is known for its versatility in the synthesis of various drugs and biologically active compounds.
  • Bioactivity: Research indicates that compounds similar to 5-methyl-6-phenyl-morpholin-3-one exhibit potential antimicrobial and antitumor properties, making them of interest in medicinal chemistry.
  • Synthetic Pathways: Scientists are increasingly exploring novel synthetic routes to develop derivatives of morpholinone that may enhance efficacy or reduce side effects.
  • Applications: Beyond pharmaceuticals, derivatives of this compound may play roles in agrochemicals and cosmetics, illustrating its industrial significance.
  • Research Opportunities: The ongoing studies into the biological functions of morpholinones suggest a vast potential for discovering new therapeutic agents, making this a rich area for scientific exploration.

As the field of medicinal chemistry continues to evolve, compounds like 5-methyl-6-phenyl-morpholin-3-one highlight the importance of structure-activity relationships in drug design and development. Each new insight brings us closer to leveraging these compounds for real-world applications, potentially leading to breakthrough treatments in medicine.

Synonyms
FENMETRAMIDE
5588-29-4
5-methyl-6-phenylmorpholin-3-one
Feninetramide
McN-1075
3-Morpholinone, 5-methyl-6-phenyl-
5-Methyl-6-phenyl-3-morpholinone
MLS003106726
NSC169876
NSC-169876
Fenmetramida
5-methyl-6-phenyl-morpholin-3-one
Fenmetramide (USAN/INN)
CHEMBL2106282
DTXSID00863576
UJEPHPADGSWWRM-UHFFFAOYSA-N
AKOS006272562
SMR001821618
DS-002547
NS00113919
D04153
EN300-212947
Q5443510