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Bisnorbenzomorphan

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Identification
Molecular formula
C36H56N2
CAS number
1622-62-4
IUPAC name
3-benzyl-9-[6-(3-benzyl-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonan-9-yl)hexyl]-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonane
State
State

At room temperature, Bisnorbenzomorphan exists as a solid due to its large molecular structure which results in strong intermolecular forces.

Melting point (Celsius)
245.00
Melting point (Kelvin)
518.00
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.00
General information
Molecular weight
556.86g/mol
Molar mass
556.8150g/mol
Density
1.1400g/cm3
Appearence

Bisnorbenzomorphan typically appears as a colorless or pale yellow solid. Its precise coloring can vary slightly depending on purity and the presence of any impurities.

Comment on solubility

Solubility of 3-benzyl-9-[6-(3-benzyl-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonan-9-yl)hexyl]-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonane

The solubility of this compound is influenced by several factors due to its complex structure. Here are some key aspects to consider:

  • Polarity: The presence of aza groups suggests that the compound is polar. This could enhance its solubility in polar solvents such as water.
  • Hydrophobic Portions: The multiple benzyl groups indicate hydrophobic characteristics, which may reduce solubility in water but enhance solubility in organic solvents.
  • Conformational Flexibility: The bicyclic structure may allow for more conformational flexibility, potentially influencing solubility in various mediums.
  • Temperature Effects: Temperature adjustments could impact solubility as the compound might dissolve better at elevated temperatures.

Overall, while the compound has polar attributes that could improve solubility in aqueous solutions, its hydrophobic regions indicate that it might be better suited for organic solvents. Thus, a careful examination of solvent choice is crucial for achieving optimal solubility. As a guiding quote in solubility studies goes, “Like dissolves like,” which reminds us to consider the molecular characteristics and interactions between solvents and solutes.

Interesting facts

Interesting Facts about 3-benzyl-9-[6-(3-benzyl-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonan-9-yl)hexyl]-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonane

This compound is a member of the aza-bicyclo[3.3.1] family, known for its intriguing structural properties and potential applications in the field of medicinal chemistry. Here are some notable aspects:

  • Complex Structure: The compound possesses a unique bicyclic framework that contributes to its high level of structural complexity. This allows for interesting interactions at the molecular level.
  • Biological Significance: As an aza-derivative, this compound might exhibit biological activities, making it of interest for pharmaceutical development. Compounds in this class have been studied for their potential in targeting various biological pathways.
  • Potential Applications: The functional groups, particularly the benzyl substituents, could enhance interactions with biological macromolecules, leading to potential uses in drug design, such as in anti-cancer or neuropharmacological applications.
  • Research Interest: Scientists are actively exploring azabicyclic compounds for their synthetic versatility and ability to mimic natural alkaloids. This makes it a fascinating area of research with expansive possibilities.
  • Synthetic Pathways: The synthesis of compounds like this one typically involves intricate multi-step processes, which can include a variety of organic transformations, making them ideal for graduate studies in synthetic organic chemistry.

In summary, the compound 3-benzyl-9-[6-(3-benzyl-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonan-9-yl)hexyl]-9-methyl-3-aza-9-azoniabicyclo[3.3.1]nonane represents a rich area of study in chemistry, bridging the realms of molecular structure, biological activity, and synthetic methodology. As researchers continue to unravel its potential, this compound may lead to exciting discoveries in the chemical and medicinal fields.