Interesting facts
Interesting Facts about (13-methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta [a] phenanthren-17-yl) propanoate
This compound, known for its complex structure and intriguing characteristics, offers a fascinating glimpse into the world of organic chemistry. Here are some enlightening insights about it:
- Structural Complexity: The compound features a multi-ring structure, typical of many steroids and complex organic molecules. Its decahydrocyclopenta[a]phenanthrene framework adds to its unique properties and behavior in various chemical environments.
- Functional Groups: The presence of a propanoyloxy group suggests the potential for interesting reactivity. This functional group can undergo reactions such as esterification and hydrolysis, making it notable in synthetic organic chemistry.
- Anticipated Applications: Compounds with similar structures are often studied for their biological activity. This could include anti-inflammatory, anabolic, or even anticancer properties, highlighting the importance of such compounds in medicinal chemistry.
- Nature of Synthesis: The synthesis of such complex molecules often involves multiple steps. Techniques like ring closure reactions, asymmetric synthesis, and protective group strategies might be employed, providing students and chemists alike a valuable learning experience.
- Historical Context: Compounds in this structural family have been synthesized and studied since the mid-20th century, with many leading to the development of various pharmaceuticals. Understanding their synthesis and properties can illuminate the evolution of modern medicinal compounds.
In summary, the intriguing (13-methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta [a] phenanthren-17-yl) propanoate not only exemplifies the beauty of organic synthesis but also potentially opens doors to future medicinal advancements.
Synonyms
17-BETA-ESTRADIOL3,17-DIPROPIONATE
Oprea1_555259
Estra-1,3,5(10)-triene-3,17-diol (17.beta.)-, dipropanoate
CHEMBL4787734
DTXSID50859202
beta -Estradiol 3,17-dipropionate
STK366310
AKOS005443350
DS-017210
estra-1(10),2,4-triene-3,17-diyl dipropanoate
estra-1,3,5(10)-triene-3,17-diyl dipropanoate
Solubility of (13-methyl-3-propanoyloxy-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl) propanoate
The solubility of the compound C22H32O3 can be influenced by various factors, including its molecular structure and interactions with solvents. Here are some key points regarding its solubility:
Summarily, while C22H32O3 may dissolve in polar solvents due to its functional groups, its hydrophobic features and bulky structure suggest limited solubility in water, supporting a preference for non-polar organic solvents. Therefore, when considering solvent choices, it is crucial to balance polarity and molecular structure for optimal solubility results.