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4-(5-morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine

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Identification
Molecular formula
C12H18N2O2S2
CAS number
.
IUPAC name
4-(5-morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine
State
State

At room temperature, the compound exists in a solid state. The structure of the compound, which includes a rigid aromatic system as well as ionic characteristics, primarily contributes to its solid state at standard conditions.

Melting point (Celsius)
125.00
Melting point (Kelvin)
398.15
Boiling point (Celsius)
332.00
Boiling point (Kelvin)
605.15
General information
Molecular weight
306.45g/mol
Molar mass
306.4460g/mol
Density
1.3400g/cm3
Appearence

The compound is typically observed as a crystalline solid. The crystals may often appear as colorless or take on a light yellow hue depending on how pure the sample is and the specific form in which the compound crystallizes. Morpholine-derived compounds can sometimes hold a slight sheen or translucence.

Comment on solubility

Solubility of 4-(5-morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine

The compound 4-(5-morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine displays interesting solubility characteristics influenced by its unique structural features. As a quaternary ammonium compound, it tends to have increased solubility in polar solvents, primarily due to the presence of multiple heteroatoms that can engage in hydrogen bonding and dipole interactions.

In general, the solubility can be described as follows:

  • Water Solubility: This compound is likely to be soluble in water, due to its ionic nature which promotes interactions with water molecules.
  • Organic Solvents: It may exhibit variable solubility in organic solvents; polarity plays a crucial role here. Polar organic solvents will generally enhance solubility, while non-polar solvents may limit it.
  • pH Sensitivity: The solubility may also be pH-dependent, with variations in solubility observed under different acidic or basic conditions, owing to potential protonation or deprotonation of functional groups.

To summarize, the solubility of 4-(5-morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine is heavily influenced by its quaternary ammonium structure, suggesting good solubility in aqueous environments and specific polar organic solvents, while being sensitive to changes in pH. This highlights the compound's versatile applicability in various chemical contexts.

Interesting facts

Interesting Facts about 4-(5-Morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine

This intriguing compound is a fascinating example of a morpholine derivative, featuring a unique structure that enables a variety of chemical interactions. Its potential applications are vast and continue to draw the attention of researchers. Here are some captivating points to consider:

  • Versatile Reactivity: The dual morpholine units within the structure allow this compound to participate in various catalytic and biochemical processes.
  • Application Potential: Compounds with morpholine functionalities are known for their utility in pharmaceuticals, particularly in the synthesis of drugs that can target specific diseases.
  • Living Systems Interaction: The presence of the dithiol moiety enhances potential interactions with biological molecules, which is a crucial aspect in medicinal chemistry.
  • Stability and Solubility: Morpholines are often recognized for their stability under various conditions, making them valuable in both laboratory and industrial settings.
  • Research Interest: This compound is currently gaining traction in research focused on the development of new therapeutic agents and the exploration of novel chemical pathways.

In summary, the compound 4-(5-morpholin-4-ium-4-ylidenedithiol-3-yl)morpholine not only embodies unique chemical properties but also illustrates the interconnectedness of chemistry with health sciences. It serves as a prime example of how chemical structures can open doors to innovative solutions in drug development.

Synonyms
NCI60_006718
SCHEMBL9353846
CHEMBL2007819