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Methyl Isocembrol

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Identification
Molecular formula
C20H32O2
CAS number
65113-99-7
IUPAC name
methyl (1R,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate
State
State

At room temperature, Methyl Isocembrol exists as a viscous liquid. Its high boiling point indicates stability in liquid form under normal conditions.

Melting point (Celsius)
32.00
Melting point (Kelvin)
305.15
Boiling point (Celsius)
287.00
Boiling point (Kelvin)
560.15
General information
Molecular weight
304.47g/mol
Molar mass
304.4670g/mol
Density
1.0276g/cm3
Appearence

Methyl Isocembrol typically appears as a colorless or pale yellow liquid. Being a derivative of naturally occurring compounds, its precise appearance might slightly vary depending on purity and source, but generally it tends to be a clear and viscous fluid.

Comment on solubility

Solubility of Methyl (1R,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate

The solubility of methyl (1R,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate can vary significantly based on several factors. Understanding these factors is crucial for applications in chemical synthesis and formulation.

Factors Affecting Solubility:

  • Polar vs. Nonpolar Solvents: This compound, being largely organic in nature, is expected to have higher solubility in nonpolar solvents such as hexane or toluene compared to polar solvents like water.
  • Temperature: Increased temperature generally enhances solubility, allowing for greater dissolution of the compound in the solvent.
  • Presence of Functional Groups: The carboxylate functional group may exhibit some degree of solubility in polar environments, but the overall hydrophobic nature of the compound might limit its extent.

As a rule of thumb, it can often be stated that *“like dissolves like,”* allowing for predictions about solubility based on solvent characteristics. However, due to the complex nature of this compound, empirical testing may be necessary to accurately assess its solubility in various solvents.

In summary, while specific solubility data for methyl (1R,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate may not be readily available, it is essential to conduct thorough investigation factoring in the nature of solvent, temperature, and compound structure for practical applications.

Interesting facts

Interesting Facts about Methyl (1R,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate

Methyl (1R,4aR)-7-isopropyl-1,4a-dimethyl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate is a fascinating organic compound with a variety of noteworthy features:

  • Synthetic Versatility: This compound can be used as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.
  • Chirality: The designation of (1R,4aR) indicates the presence of stereocenters, making it a chiral molecule. This chirality is crucial, as different stereoisomers can exhibit vastly different biological activities.
  • Natural Occurrence: Hydrocarbon structures similar to this compound are often found in natural products, highlighting the interconnectedness between synthetic and natural chemistry.
  • Structural Complexity: The octahydrophenanthrene core provides a robust skeletal framework, with numerous substituents allowing for diverse chemical reactivity and interactions.
  • Applications: Potential uses for this compound include applications in polymer chemistry, fragrance formulations, and as intermediates in the synthesis of more complex molecules.

In discussing this compound, it’s essential to recognize the balance between synthetic accessibility and structural intricacy. As researchers continue to explore its properties, the potential for new discoveries and innovations remains vast. As the renowned chemist Linus Pauling once said, “The best way to have a good idea is to have a lot of ideas.” This compound exemplifies how studying such complex structures can lead to groundbreaking advancements in chemistry.