Interesting facts
Interesting Facts about 17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl hexanoate
This compound is a fascinating molecule, known for its structural complexity and unique characteristics. Here are some intriguing aspects:
- Natural Product Derivative: This compound can be categorized as a derivative of a natural steroid, which showcases the intricate transformation that organic compounds can undergo in nature.
- Potential Biological Activity: Due to its structural framework, which resembles hormones and signaling molecules, it may exhibit interesting biological activities, making it a point of interest in pharmaceutical research.
- Component of Steroid Synthesis: Understanding its synthesis can provide insights into the methodologies used in steroid chemistry, which is vital for the development of various therapeutic agents.
- Synthetic Pathways: The synthesis of this compound involves multiple organic reactions, showcasing intricate strategies used by chemists to build complex structures from simpler precursors.
- In the Words of a Chemist: "The true beauty of organic chemistry lies in the vast possibilities of compound formation, making each synthesis a new adventure!"
Overall, this compound stands as a testament to the rich complexity and potential of organic chemistry. Its exploration may lead to significant discoveries in medicinal chemistry and beyond, opening doors to innovations in drug development and biochemistry.
Synonyms
3,20-Dioxopregn-4-en-17-yl hexanoate
SCHEMBL17517045
DTXSID40859514
STL356011
AKOS022096655
[(8R,9S,10R,13S,14S,17S)-17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl] hexanoate
Solubility of (17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl) hexanoate
The solubility of the compound with the formula C26H40O3 is influenced by various factors including polarity, temperature, and the presence of solvents. This compound is **relatively non-polar** due to its significant hydrocarbon structure, which implies that it may have limited solubility in polar solvents such as water.
However, it might exhibit better solubility in:
In general, the rule of thumb regarding solubility is that "like dissolves like," meaning that non-polar compounds tend to dissolve better in non-polar solvents. The presence of the acetyl and hexanoate functional groups may introduce some **moderate polarity**, but overall, the compound's substantial hydrocarbon framework will prevail in determining its solubility behavior.
It is also important to note that **temperature** can have a significant impact on solubility, especially in organic solvents. As temperature increases, solubility often enhances due to increased molecular movement.
In summary, while (17-acetyl-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl) hexanoate may demonstrate limited solubility in polar solvents, its compatibility with a wide range of organic solvents makes it versatile for various applications.