Fluocinolone acetonide
- Molecular formula
- C24H30F06
- CAS Number
- 67-73-2
- IUPAC Name
- [(17R)-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl] pentanoate
- Molecular Weight
- 452.49g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3600g/cm3
- Synonyms
- DTXSID60945948
Identification
Interesting Facts about [(17R)-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl] pentanoate
This compound, a complex derivative of steroids, presents a fascinating study for chemists and biologists alike due to its multifaceted structure and potential applications in medicine. Its intricate formulation is a testament to the beauty of organic chemistry, particularly in the modification of naturally occurring steroidal frameworks.
Key Features
- Structural Diversity: The presence of multiple functional groups such as hydroxy and fluoro makes this compound a subject of interest for synthetic organic chemistry.
- Biological Activity: Compounds like this have been studied for their potential pharmaceutical effects, particularly in relation to hormonal activity and anti-inflammatory properties.
- Synthetic Challenges: The synthesis of such a complex molecule often involves multistep reactions, which can showcase advanced techniques such as asymmetric synthesis and selective functionalization.
As with many steroid derivatives, the challenge lies not just in creating the molecule, but also in understanding its mechanism of action once synthesized. The introduction of fluorine atoms, for example, can significantly alter the compound's potency and bioavailability, and this has prompted extensive research.
Noteworthy Research Insights
- The pharmacological implications of modified steroids have led to their exploration in treatments for conditions such as cancer and autoimmune diseases.
- Environmental impact studies may investigate how these compounds behave in biological systems and their potential to bioaccumulate.
In conclusion, the investigation of [(17R)-6-fluoro-11-hydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-yl] pentanoate not only deepens our understanding of steroid chemistry but also opens doors to innovative therapeutic avenues. This compound exemplifies the intersection of structural complexity and biological relevance, making it an intriguing subject within the realm of chemical sciences.