Estrone
- Molecular formula
- C18H22O2
- CAS Number
- 53-16-7
- IUPAC Name
- (17S)-17-hydroxy-13,17-dimethyl-1,2,4,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
- Molecular Weight
- 270.37g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2300g/cm3
- Synonyms
- CCG-248771
Identification
Interesting Facts about (17S)-17-hydroxy-13,17-dimethyl-1,2,4,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
This intriguing compound, commonly recognized in the realm of organic chemistry and biochemistry, is noteworthy for its complex structure and unique properties. Here are some interesting aspects to consider:
- Synthetic Importance: This compound is a significant precursor in the synthesis of various steroids, showcasing its utility as a building block in pharmaceutical applications.
- Biological Activity: Compounds of this class often exhibit a range of biological activities, including hormonal and therapeutic effects, making them valuable in medicinal chemistry.
- Chirality: The ā17Sā designation indicates that this molecule possesses chirality, which can influence its biological interactions and pharmacokinetic properties.
- Structural Complexity: With its intricate ring structure, the compound is a part of the larger family of polycyclic compounds, known for their rich chemical behavior.
- Potential Research Applications: Researchers often explore the potential of such compounds in cancer treatment and other diseases, given their steroidal nature.
As one delves deeper into the study of this compound, it becomes clear that its multifaceted nature presents an exciting area for ongoing research and exploration.
In the words of chemist George A. Olah, "The complexity of organic compounds embodies the beauty of chemistry." This truism holds especially true for (17S)-17-hydroxy-13,17-dimethyl-1,2,4,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one, exemplifying the intricate relationships between structure and function in organic molecules.