Testosterone tosylate

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Identification

Molecular formula
C27H38O4S
CAS Number
3653-06-9
IUPAC Name
[10,13-dimethyl-17-(1-methylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate
Molecular Weight
502.66g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.0800g/cm3
Synonyms
(10, 13-dimethyl-17-octan-2-yl-2, 3, 4, 5, 6, 7, 8, 9, 11, 12, 14, 15, 16, 17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl) 4-methylbenzenesulfonate
Interesting facts

Interesting Facts about [10,13-Dimethyl-17-(1-methylheptyl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] 4-methylbenzenesulfonate

This compound, with its intricate and extended chemical structure, belongs to a class of compounds known for their unique biochemical interactions. Here are some engaging facts about it:

  • Synthetic Nature: This compound is a synthetic derivative often utilized in the study of receptor binding and pharmacological activities, providing insight into mechanisms of action in various biological systems.
  • Unique Structure: The complex cyclopenta[a]phenanthrene backbone gives this compound interesting attributes, enabling it to interact with numerous targets in the body, such as steroid receptors.
  • Potential Applications: Due to its structure, it may be explored for its potential therapeutic effects, particularly in the fields of endocrinology and cancer research.
  • Substituents Matter: The presence of the 4-methylbenzenesulfonate group can enhance solubility properties and could influence how this compound behaves in biological systems, making it a vital area of research.

As with many compounds of this nature, structure-activity relationships play a crucial role in understanding its effects. Researchers continually aim to uncover the depths of its function:

"Understanding the nuances of molecular interactions is key to unlocking therapeutic potential." - Anonymous

Overall, the compound reflects the fascinating complexity of organic chemistry, bridging synthetic methods with potential real-world applications in medicine and beyond.

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