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Acetylated androsterone

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Identification
Molecular formula
C25H36O5
CAS number
1239-45-8
IUPAC name
[(17S)-1,3-diacetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] acetate
State
State

At room temperature, acetylated androsterone is typically in a solid state. Its crystalline nature makes it stable under normal conditions provided it is stored appropriately.

Melting point (Celsius)
138.00
Melting point (Kelvin)
411.15
Boiling point (Celsius)
340.00
Boiling point (Kelvin)
613.15
General information
Molecular weight
396.55g/mol
Molar mass
396.5540g/mol
Density
1.1509g/cm3
Appearence

Acetylated androsterone typically appears as a white to off-white crystalline powder. It is odorless and can be identified by its distinct crystalline texture.

Interesting facts

Interesting Facts about [(17S)-1,3-diacetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] Acetate

[(17S)-1,3-diacetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] acetate is a fascinating compound with a rich background in both natural and synthetic chemistry. Here are some intriguing points to consider:

  • Steroidal Structure: This compound is part of a larger family of steroids, which are known for their diverse biological activities. The complex cyclic structure contributes to its unique properties.
  • Biochemical Interest: Its structure indicates potential interactions with biological systems, making it a candidate for studies in pharmacology and biochemistry.
  • Role in Medicine: Analogous compounds in the steroid family have been used in medicine for their anti-inflammatory and anabolic properties, paving the way for assorted therapeutic applications.
  • Development of Synthetic Methods: The synthesis of such complicated molecules can improve synthetic techniques, which can be applied to the production of various biologically active substances.
  • Environmental Relevance: Studying compounds like this one may provide insights into the metabolism of natural steroids and their environmental impact.

It’s also noteworthy to mention the various synthesis pathways scientists employ when creating such molecules, including functional group manipulation and cis-trans isomerization. As a chemistry student or researcher, understanding the properties and potential applications of such compounds can open up new avenues in both research and practical applications.

As the world of chemistry continues to evolve, learning about compounds like [(17S)-1,3-diacetoxy-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl] acetate not only enriches our understanding of molecular interactions but also inspires innovations in understanding and treating various health conditions.

Synonyms
4248-03-7
ESTRA-1,3,5(10)-TRIENE-1,3,17-beta-TRIOL, TRIACETATE
DTXSID30962526
Estra-1(10),2,4-triene-1,3,17-triyl triacetate