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Oxomemazine

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Identification
Molecular formula
C17H25ClN2O2
CAS number
3692-81-7
IUPAC name
3,5,7-trimethyl-1-(2-morpholin-4-ium-2-ylethyl)-3H-azepin-2-one;chloride
State
State

At room temperature, Oxomemazine hydrochloride is a solid. It is stable under normal conditions and is typically formulated into tablets or other dosage forms for medicinal use.

Melting point (Celsius)
204.00
Melting point (Kelvin)
477.15
Boiling point (Celsius)
417.00
Boiling point (Kelvin)
690.15
General information
Molecular weight
354.89g/mol
Molar mass
354.8890g/mol
Density
1.2807g/cm3
Appearence

Oxomemazine hydrochloride typically appears as a white or off-white crystalline powder. The compound is often used in finely milled form for pharmaceutical applications.

Comment on solubility

Solubility of 3,5,7-trimethyl-1-(2-morpholin-4-ium-2-ylethyl)-3H-azepin-2-one;chloride

The compound 3,5,7-trimethyl-1-(2-morpholin-4-ium-2-ylethyl)-3H-azepin-2-one;chloride exhibits interesting solubility properties that can be largely attributed to its ionic nature and molecular structure.

Factors Affecting Solubility

  • Ionic Characteristics: Being a chloride, it may exhibit good solubility in polar solvents such as water due to the presence of chlorine atoms that can interact with the solvent molecules.
  • Hydrogen Bonding: The morpholine group can form intermolecular hydrogen bonds, which can enhance solubility, especially in polar protic solvents.
  • Alkyl Substituents: The three methyl groups could lead to conflicting effects; while they may increase lipophilicity, they can also reduce the overall solubility in purely aqueous environments.

Therefore, the solubility of this compound can be characterized as:

  • High in Polar Solvents: It is likely to dissolve well in water and alcohols due to ionic and polar interactions.
  • Limited in Non-Polar Solvents: Solubility in non-polar solvents such as hexane would be very low due to the lack of suitable interactions.

In summary, one could say, "Solubility is a dance of interactions where the right partners create harmony!" The behavior of 3,5,7-trimethyl-1-(2-morpholin-4-ium-2-ylethyl)-3H-azepin-2-one;chloride in different solvents showcases the importance of molecular structure in determining chemical behavior.

Interesting facts

Interesting Facts about 3,5,7-Trimethyl-1-(2-morpholin-4-ium-2-ylethyl)-3H-azepin-2-one; Chloride

This fascinating compound is part of a broader class of organic compounds, known for its unique structure and potential applications. Here are some notable insights:

  • Complex Structure: The compound features a 3H-azepin core, which is a seven-membered saturated ring. This cyclic structure contributes to the compound's intriguing properties and potential reactivity.
  • Morpholine Derivative: The presence of a morpholine group introduces a nitrogen-containing heterocycle, enhancing the biological activity of the compound. Morpholines are well-known for their roles in pharmacology, particularly in drug design.
  • Trimethyl Substitution: The three methyl groups at positions 3, 5, and 7 significantly influence the compound's chemical behaviors, including its polarity and steric effects. This branched structure can affect how the compound interacts with biological targets.
  • Potential in Medicinal Chemistry: Research indicates that similar compounds may exhibit antibacterial, antifungal, or antitumor activities, opening doors for further exploration in pharmaceutical applications.
  • Chloride Salt: Being in a chloride form suggests enhanced solubility and stability, often facilitating its use in various chemical reactions and as an intermediary in synthesis pathways.

In summary, the unique combination of features within this compound not only emphasizes its chemical diversity but also highlights the potential for significant contributions to medicinal chemistry and related fields. The impact of such compounds can be profound, paving the way for innovations that could enhance health and well-being.

Synonyms
2H-Azepin-2-one, 1,3-dihydro-1-(2-morpholinoethyl)-3,5,7-trimethyl-, hydrochloride
1-(2-Morpholinoethyl)-1,3-dihydro-3,5,7-trimethyl-2H-azepin-2-one hydrochloride
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