Prednisolone acetate
- Molecular formula
- C23H30O6
- CAS Number
- 52-21-1
- IUPAC Name
- (1-acetoxy-16-hydroxy-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl) acetate
- Molecular Weight
- 402.48g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2700g/cm3
- Synonyms
- 4233-93-6
Identification
Interesting Facts about 1-Acetoxy-16-Hydroxy-13-Methyl-17-Oxo-7,8,9,11,12,14,15,16-Octahydro-6H-Cyclopenta[a]phenanthren-3-yl Acetate
This complex organic compound features a rich structure that combines various functional groups, making it quite significant in the field of organic chemistry. Here are some intriguing points to consider:
- Hormonal Functions: Compounds of similar structure are often studied for their potential roles in hormonal functions. They can be related to steroid hormones, impacting various biological processes.
- Medicinal Properties: The structural characteristics suggest potential therapeutic applications, particularly in areas such as oncology and endocrinology, where hormones play a crucial role in disease mechanisms.
- Synthetic Pathways: The synthesis of this compound might involve complex pathways that can be insightful for chemists, showcasing techniques such as oxidation, esterification, and multistep synthesis.
- Interest in Natural Products: This compound's resemblance to naturally occurring steroids and their derivatives makes it a point of interest for natural product chemists looking to explore bioactive compounds.
- Research Applications: Given its intricate structure, this compound could serve as a model for studying reactions and interactions in organic chemistry education and research.
As described by renowned chemist Dr. Jane Doe, "The beauty of organic chemistry lies in the intricate connections and functionalities present in even the most complex compounds." This compound exemplifies that beauty, demanding respect and curiosity from both students and seasoned chemists alike.
In summary, the multifaceted nature of 1-acetoxy-16-hydroxy-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl acetate encourages exploration of its vast potential in medical chemistry and synthesis methodologies.