Testosterone propionate

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Identification

Molecular formula
C22H32O3
CAS Number
57-85-2
IUPAC Name
[(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl] propanoate
Molecular Weight
344.49g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0800g/cm3
Synonyms
Bolandiol dipropionate
Interesting facts

Interesting Facts about [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopentaphenanthren-3-yl] propanoate

This compound, a complex derivative of the steroid family, presents fascinating aspects worth exploring. Its structure boasts of multiple stereocenters, specifically at the 3 and 17 positions, leading to unique stereochemistry that can influence its biological activity.

Key Features:

  • Biological Relevance: This compound may have implications in drug development, particularly due to its relation to steroid-like compounds.
  • Synthesis Potential: The intricate structure poses challenges and opportunities for organic synthesis; chemists continue to refine methods to construct such complex frameworks.
  • Pharmacological Properties: As a derivative of steroid compounds, it may exhibit hormonal activity, opening pathways for therapeutic applications in areas such as endocrinology and oncology.

Research indicates that compounds like this often interact with cellular receptors, thereby influencing various biological pathways. As emphasized by many chemists, understanding the nuances in structure can unlock significant breakthroughs in medicinal chemistry.

In summary, the study of [(3S,17S)-13-methyl-17-propanoyloxy-1,2,3,6,7,8,9,10,11,12,14,15,16,17-tetradecahydrocyclopentaphenanthren-3-yl] propanoate not only enhances our comprehension of complex organic molecules but also emphasizes the intricacies involved in drug design and development. The journey through its synthesis and potential applications certainly keeps chemists intrigued!

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