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Presumably a synthetic steroid compound

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Identification
Molecular formula
C25H34O5
CAS number
/
IUPAC name
(10,13-dimethyl-3-oxo-2-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) propanoate
State
State
Solid
Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
418.54g/mol
Molar mass
418.5910g/mol
Density
1.1000g/cm3
Appearence

The compound is likely a crystalline solid at room temperature, typical of many steroid derivatives. The color may range from white to off-white.

Comment on solubility

Solubility Insights

The compound (10,13-dimethyl-3-oxo-2-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopentaphenanthren-17-yl) propanoate exhibits notable characteristics regarding its solubility.

Factors Affecting Solubility

Understanding the solubility of this complex organic compound involves several key factors:

  • Polarity: The presence of functional groups, such as the propanoyloxy group, impacts polarity, enhancing solubility in polar solvents.
  • Hydrogen Bonding: The molecule can potentially participate in hydrogen bonding, thus affecting solubility in various solvents.
  • Size and Structure: The intricate structure of the compound may restrict its solubility in water, common for larger organic molecules.

Solubility Predictions

Generally, one might expect this compound to be:

  • More soluble in organic solvents: Such as ethanol, acetone, and dichloromethane.
  • Poorly soluble in water: Due to its hydrophobic components and sterically hindered structure.

In conclusion, predicting solubility can often provide insights into the compound's behavior in various chemical environments. It’s essential to conduct empirical testing to determine precise solubility values, as theoretical predictions might not capture all nuances.

Interesting facts

Interesting Facts about 10,13-Dimethyl-3-oxo-2-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-Dodecahydrocyclopenta[a]phenanthren-17-yl Propanoate

This compound, with its complex structure, is a fascinating example of the interplay between organic chemistry and medicinal applications. Here are some intriguing points regarding this specific compound:

  • Structure Complexity: The molecular structure of this compound is characterized by multiple rings and functional groups, which can lead to unique chemical behavior and properties. Its intricate arrangement can be a subject of study in stereochemistry.
  • Medical Relevance: Compounds similar in structure to this one are often explored for their potential therapeutic effects. Research into cyclopenta[a]phenanthrene derivatives has shown promise in various fields, including oncology and endocrinology.
  • Natural Occurrence: Many compounds with a phenanthrene core are found in nature, especially in certain plants and fungi. This connection indicates a potential for discovering new pharmaceuticals that leverage natural biosynthesis.
  • Synthesis Challenges: Creating such complex organic compounds often requires innovative synthetic pathways. Scientists typically employ multi-step synthesis, utilizing various reactions like oxidation, acylation, and cyclization to assemble the final product.
  • Analytical Techniques: To study and verify the structure of this compound, chemists often deploy advanced analytical techniques such as NMR spectroscopy and mass spectrometry. These tools are vital for understanding the unique properties and behaviors of complex chemicals.
  • Research Frontiers: Ongoing research seeks to evaluate the biological activity of similar compounds, potentially leading to new discoveries in drug design. Investigating the interaction of these compounds at the molecular level can uncover mechanisms that may inform therapeutic strategies.

In summary, the exploration of 10,13-dimethyl-3-oxo-2-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl propanoate opens up several avenues for further investigation in both organic chemistry and pharmaceutical development. As we delve deeper into such compounds, who knows what groundbreaking treatments or technologies may arise?

Synonyms
22204-96-2
2-ALPHA-HYDROXYTESTOSTERONE DIPROPIONATE
(10,13-dimethyl-3-oxo-2-propanoyloxy-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) propanoate
NSC-12204
DTXSID10944865
NSC12204
2.alpha.-Hydroxytestosterone propionate
2-.alpha.-hydroxytestosterone dipropionate
2.alpha.-Hydroxytestosterone, dipropionate
3-oxoandrost-4-ene-2,17-diyl dipropanoate
Androst-4-en-3-one,17.beta.-dihydroxy-, dipropionate
2-.alpha.-17-.beta.-bis(1-oxopropoxy)androst-4-en-3-one
2-.alpha.-17-.beta.-dihydroxyandrost-4-en-3-one dipropionate
Androst-4-en-3-one,17-bis(1-oxopropoxy)-, (2.alpha.,17.beta.)-