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4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide

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Identification
Molecular formula
C23H30BrNO
CAS number
.
IUPAC name
4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one;bromide
State
State

At room temperature, 4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide is typically in a solid state, often in crystalline or powdered form.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
440.36g/mol
Molar mass
440.3620g/mol
Density
1.2000g/cm3
Appearence

4,4-Diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide appears as an off-white to white crystalline solid. It is typically found in the form of a fine powder.

Comment on solubility

Solubility of 4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide

The solubility of 4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide can significantly influence its applications in both research and industry. Here are some key points regarding its solubility characteristics:

  • Solvent Influence: The solubility of the compound is heavily dependent on the choice of solvent. Commonly, it tends to dissolve better in polar solvents due to its ionic nature.
  • Ionic Interaction: As a bromide salt, the ionic bond between the bromide ion and the cationic part of the molecule can promote dissolution in polar media.
  • Temperature Effects: Increasing the temperature typically enhances the solubility of ionic compounds, making it easier for this compound to dissolve in suitable solvents.

However, while the compound has favorable solubility in certain polar solvents, it may exhibit limited solubility in non-polar solvents. This can affect its utilization in various applications, which is crucial to consider during formulation. Understanding these solubility parameters can help in the effective use and manipulation of this compound in chemical processes.

Interesting facts

Interesting Facts about 4,4-Diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one Bromide

The compound known as 4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide is an intriguing example of an ionic compound with applications in various fields, particularly in medicinal chemistry and organic synthesis. Here are some key points that showcase its significance:

  • Structural Characteristics: This compound features a complex structure with a piperidinium ring, which is notable for its role in the development of various pharmaceuticals. The presence of diphenyl groups contributes to its chemical stability and versatility.
  • Biological Activity: Compounds of this nature often exhibit biological properties, making them valuable in drug discovery. They can interact with biological systems, potentially influencing receptor activity and providing therapeutic benefits.
  • Solubility and Ion Exchange: As a bromide salt, it exhibits unique solubility characteristics that can be advantageous in various solvents, enhancing its usability in chemical reactions and analysis.
  • Research Applications: Its structural complexity allows it to serve as a useful molecular scaffold in synthetic chemistry, facilitating the creation of new compounds with desirable properties.
  • Encapsulation Potential: The ionic nature of the compound may allow it to form complexes with other substances, making it a candidate for encapsulation in nanoscale applications.

In summary, the multifaceted roles of 4,4-diphenyl-6-piperidin-1-ium-1-yl-hexan-3-one bromide in medicinal chemistry and synthesis highlight the importance of exploring such compounds in greater detail. As scientists continue to uncover their potential, this compound could lead to significant advancements in various fields.

Synonyms
Hexalgon hydrobromide
P3815G1KRY
UNII-P3815G1KRY
4,4-Diphenyl-6-piperidino-3-hexanone hydrobromide
6-Piperidino-4,4-diphenylhexan-3-one hydrobromide
1-Piperidino-3,3-diphenylhexan-4-on hydrobromid [German]
3-HEXANONE, 4,4-DIPHENYL-6-PIPERIDINO-, HYDROBROMIDE
1-Piperidino-3,3-diphenylhexan-4-on hydrobromid