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Testosterone adamantyl ester

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Identification
Molecular formula
C32H44O3
CAS number
null
IUPAC name
[(9S,14S,17S)-13-methyl-3-oxo-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl] adamantane-1-carboxylate
State
State

At room temperature, Testosterone adamantyl ester is typically in a solid state. It is stable under normal conditions and does not readily evaporate or melt at ambient temperatures.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
288.00
Boiling point (Kelvin)
561.15
General information
Molecular weight
475.69g/mol
Molar mass
475.6910g/mol
Density
1.1800g/cm3
Appearence

Testosterone adamantyl ester appears as a white crystalline solid. Its exact crystalline structure may vary, but it typically presents as a fine powder or small white crystals.

Comment on solubility

Solubility Overview

The solubility of [(9S,14S,17S)-13-methyl-3-oxo-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopentaphenanthren-17-yl] adamantane-1-carboxylate can be quite complex due to its intricate molecular structure. Here are some key considerations regarding its solubility:

Factors Influencing Solubility:

  • Molecular Structure: The presence of the adamantane and cyclopentaphenanthren moieties can significantly impact how this compound interacts with solvents.
  • Polarity: Non-polar regions of the molecular structure may lead to lower solubility in polar solvents, while potential polar functional groups could promote solubility in non-polar solvents.
  • Temperature: Solubility may increase with temperature, making it more soluble in hot solvents compared to cold.

Solvent Compatibility:

In general, the solubility of complex organic compounds like this one tends to be:

  • Higher in organic solvents: Such as dichloromethane, ethanol, and acetone, due to their compatibility with non-polar structures.
  • Lower in water: Given the compound's predominantly hydrophobic nature, it is likely to have low solubility in aqueous solutions.

As with many organic compounds, the **exact solubility can vary** widely depending on the specific conditions and solutes involved. It is always advisable to conduct empirical measurements for precise solubility data.

Interesting facts

Interesting Facts about [(9S,14S,17S)-13-methyl-3-oxo-2,6,7,8,9,10,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl] adamantane-1-carboxylate

This compound, with its intricate structure, is a fascinating example of how complex organic molecules can be synthesized. Here are some intriguing aspects:

  • Synthetic Importance: The structure showcases a unique combination of cyclic and polycyclic frameworks, making it a subject of interest in synthetic organic chemistry.
  • Potential Applications: Due to its intricate configuration, the compound could be explored for uses in pharmaceuticals, potentially exhibiting biological activity or serving as a precursor for drug synthesis.
  • Stereochemistry: The specific stereochemical designations (9S, 14S, 17S) indicate that this compound possesses chiral centers, which are crucial in determining the biological activity and interactions of many organic molecules.
  • Comparison with Similar Compounds: The resemblance to hormone-like compounds, such as steroids, makes it an interesting candidate for investigations into hormone analogues or inhibitors.
  • Research Opportunities: Students and researchers can explore the compound's reactivity, stability, and methods for its synthesis, offering numerous avenues for experimentation and education.

As you delve into the world of organic compounds like this one, remember the words of renowned chemist Marie Curie: "Nothing in life is to be feared; it is only to be understood." Exploring such complex structures deepens our understanding of chemistry and its myriad possibilities.


Synonyms
NS00123697