Skip to main content

Adrenosterone

ADVERTISEMENT
Identification
Molecular formula
C19H24O2
CAS number
382-45-6
IUPAC name
10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one
State
State

Adrenosterone is a solid at room temperature.

Melting point (Celsius)
197.00
Melting point (Kelvin)
470.15
Boiling point (Celsius)
455.00
Boiling point (Kelvin)
728.15
General information
Molecular weight
300.43g/mol
Molar mass
300.4340g/mol
Density
1.2000g/cm3
Appearence

Adrenosterone typically appears as a white to off-white crystalline powder.

Comment on solubility

Solubility of 10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one

The solubility of 10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one is influenced by its complex molecular structure, which contains extensive hydrocarbon chains. Generally speaking, compounds that are primarily hydrophobic, like this one, tend to exhibit low solubility in polar solvents such as water. Here are some key points to consider:

  • Solvent Type: This compound may dissolve better in non-polar solvents such as hexane or chloroform, due to the hydrophobic nature of its framework.
  • Temperature Effects: Increased temperature can enhance solubility in organic solvents by increasing kinetic energy and reducing intermolecular forces.
  • Potential Applications: Understanding solubility is crucial for its application in various organic reactions and formulations in the chemical industry.

To summarize, the solubility of 10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one is primarily limited in polar environments but may exhibit better dissolvability in non-polar organic solvents, making it suitable for specific chemical applications.

Interesting facts

Interesting Facts about 10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one

This intriguing compound, often discussed in the realm of organic chemistry, possesses a rich structure that lends itself to a variety of fascinating applications. Here are some noteworthy aspects to consider:

  • Structural Complexity: The unique arrangement of its rings indicates a specific stereochemistry that significantly affects its reactivity and interaction with other molecules.
  • Natural Occurrence: Compounds similar in structure are often found in various natural sources, particularly in steroidal frameworks and some forms of plant secondary metabolites.
  • Biological Relevance: Research has indicated that similar structures may exhibit biological activity, potentially acting as precursors to hormones or other biologically significant molecules.
  • Synthesis Challenges: The synthesis of this compound often involves intricate multi-step reactions, showcasing the skill and precision required in organic synthesis.
  • Analytical Techniques: Characterization of this compound can utilize advanced methods such as NMR spectroscopy and mass spectrometry, crucial for confirming its structure and purity.
  • Potential Applications: Understanding the reactivity of its functional groups can lead to applications in pharmaceuticals, materials science, or as intermediates in organic synthesis.

In the words of a seasoned chemist, “The beauty of chemistry lies not just in its products, but in the journey of synthesis and discovery.” This compound exemplifies that sentiment profoundly.

Exploring the intricacies of 10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one can lead to new insights into chemical behavior and potential innovations in various scientific fields.

Synonyms
10,17,17-trimethyl-1,2,6,7,8,9,11,12,15,16-decahydrocyclopenta[a]phenanthren-3-one
23257-23-0
DIMETHYLNORANDROSTADIENONE
DTXSID60274927
10,17,17-trimethylgona-4,13-dien-3-one