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Tetrahydrocannabinol acetate

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Identification
Molecular formula
C23H32O3
CAS number
23132-17-4
IUPAC name
[17-(4-ethyl-1,5-dimethyl-hex-2-enyl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate
State
State

This compound is a liquid at room temperature, often described as an oil due to its viscous nature.

Melting point (Celsius)
-89.00
Melting point (Kelvin)
184.15
Boiling point (Celsius)
220.00
Boiling point (Kelvin)
493.15
General information
Molecular weight
368.57g/mol
Molar mass
368.5730g/mol
Density
0.9200g/cm3
Appearence

A viscous oil that is typically colorless to amber. It may appear slightly yellowish under certain lighting conditions.

Comment on solubility

Solubility of [17-(4-ethyl-1,5-dimethyl-hex-2-enyl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

The solubility of the compound [17-(4-ethyl-1,5-dimethyl-hex-2-enyl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate can be influenced by various factors, owing to its complex molecular structure. It is essential to consider the following aspects:

  • Polarity: The presence of both hydrophobic and hydrophilic regions in this molecule can lead to variable solubility in different solvents. Generally, compounds with more hydrophobic characteristics tend to be less soluble in water but may dissolve better in organic solvents.
  • Temperature: Increasing temperature typically enhances solubility. Thus, conducting solubility experiments at varying temperatures may yield different results.
  • pH Level: For compounds that can ionize, the pH of the solvent can significantly affect solubility. It’s crucial to measure solubility across different pH ranges.
  • Solvent Nature: Solvent interactions are vital; polar solvents (like water) generally dissolve polar compounds well, while non-polar solvents are more effective for non-polar compounds.

In the case of this acetate, solubility should be explored in various organic solvents (like ethanol, methanol, or dichloromethane), as the acetate moiety might provide some solubility compared to similar structures without this functional group. Additionally, it is pivotal to conduct empirical studies to establish a clear solubility profile.

As a reminder, solubility is a multifaceted property that can be affected by several concurrent factors, and understanding these can be crucial for practical applications.

Interesting facts

Interesting Facts about [17-(4-ethyl-1,5-dimethyl-hex-2-enyl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate

This complex compound is primarily associated with the field of organic chemistry and has garnered interest due to its structural intricacies and potential applications. Here are some fascinating insights about this compound:

  • Structural Complexity: The compound features a robust polycyclic framework, which is a hallmark of many biologically active molecules. Its structure consists of a hydrophobic dodecahydro-cyclopenta[a]phenanthrene core, making it an intriguing subject for studies in chemical synthesis and structure-activity relationships.
  • Synthetic Applications: Compounds of this nature are often studied for their roles in synthetic organic chemistry. The various functional groups present can lead to unique reactivity, making them useful in multi-step synthesis for creating more intricate molecules.
  • Biological Relevance: Similar compounds are known to exhibit significant biological activity. While this specific molecule may not have been extensively studied, the presence of acetate groups and polycyclic structures can sometimes correlate with properties such as anti-inflammatory or hormonal activities.
  • Research Potential: The intriguing structure of this compound provides ample opportunity for future research. Chemists might explore its use in pharmaceuticals or materials science, potentially leading to the development of new drugs or innovative materials.
  • Stereochemistry: The stereochemical aspects of such compounds are crucial for their reactivity and interactions. Investigating the stereochemical outcomes of reactions involving this compound could yield valuable insights into the principles of stereochemistry and chirality in organic molecules.

In summary, the compound [17-(4-ethyl-1,5-dimethyl-hex-2-enyl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate is not simply a collection of atoms and bonds; it encapsulates a realm of opportunities for chemists and researchers alike. Embracing the challenge of synthesizing, analyzing, and potentially utilizing this compound can lead to remarkable advancements in the world of chemistry.