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Testosterone phenylpropionate

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Identification
Molecular formula
C28H36O3
CAS number
1255-49-8
IUPAC name
[(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-phenylpropanoate
State
State
At room temperature, testosterone phenylpropionate is typically a solid, specifically in a crystalline form, and is often presented as a powder for utilization in various applications.
Melting point (Celsius)
112.00
Melting point (Kelvin)
385.15
Boiling point (Celsius)
489.60
Boiling point (Kelvin)
762.80
General information
Molecular weight
406.57g/mol
Molar mass
406.5720g/mol
Density
1.0640g/cm3
Appearence

Testosterone phenylpropionate appears as a crystalline powder. Depending on the batch, its color can range from a nearly white to pale yellow, consistent with many steroidal esters. It is practically insoluble in water but is soluble in many organic solvents.

Comment on solubility

Solubility of [(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-phenylpropanoate

The solubility of this complex organic compound is influenced by several factors, primarily its molecular structure and the presence of functional groups. Understanding the solubility can be essential for its application in various fields such as pharmaceuticals or materials science. Here are key considerations regarding its solubility:

  • Polarity: The compound contains both aliphatic and aromatic regions, which affects how it interacts with solvents. Generally, compounds with non-polar sections are less soluble in polar solvents.
  • Temperature Dependence: Like many organic compounds, solubility can increase with temperature. Higher temperatures often provide more kinetic energy to break intermolecular interactions, facilitating dissolution.
  • Functional Group Influence: The presence of functional groups, such as carbonyls in the structure, can enhance solubility in polar solvents due to hydrogen bonding.
  • Solvent Compatibility: Solutions can be achieved when paired with suitable solvents, such as organic solvents (e.g., ethanol, methanol) that can accommodate its non-polar regions.
  • Concentration Variability: Solubility is also dependent on concentration; higher concentrations might lead to precipitation, indicating a limit to solubility.

As a result, one could anticipate that the solubility of this compound may vary significantly across different solvents and under varying conditions. While definitive solubility values are generally required for practical use, the outlined aspects provide a valuable framework for understanding the solubility behavior of this compound. In conclusion, effective solubility assessment can only be achieved through experimental determination in the desired medium.

Interesting facts

Interesting Facts about [(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-phenylpropanoate

This compound, often discussed within the realm of organic chemistry, presents a unique structure that highlights the fascinating diversity of chemical compounds. Here are some intriguing insights:

  • Stereochemistry: With its complex stereochemical configuration, this compound demonstrates the importance of chirality in chemical behavior. Stereoisomers can have vastly different properties, affecting everything from biological activity to reactivity.
  • Biological Relevance: Compounds like this one are often studied for their potential pharmacological applications. The structural similarities to steroid-like frameworks can lead to significant biological interactions, influencing hormone activity and metabolic processes.
  • Natural Occurrence: Many compounds with similar polycyclic structures are derived from natural sources. This highlights the role of natural products in drug discovery and development. Understanding these compounds can pave the way for synthetic analogs with enhanced efficacy.
  • Analytical Techniques: The modest complexity of the molecular structure presents numerous opportunities for analytical techniques, such as NMR spectroscopy and mass spectrometry, allowing chemists to dissect the compound’s features.
  • Potential for Synthesis: The synthesis of such multi-functional compounds can serve as a challenging yet rewarding endeavor in synthetic organic chemistry, involving advanced strategies such as functionalization and cyclization reactions.

In summary, the study of [(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-phenylpropanoate not only deepens our understanding of complex organic molecules but also emphasizes the intricate balance between structure and function in chemical compounds.

Synonyms
Testosterone phenylpropionate
Testosterone 17-phenylpropionate
Testosterone hydrocinnamate
EINECS 215-014-4
UNII-8GN84GWX51
NSC 26643
[(8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl] 3-phenylpropanoate
DTXSID5048712
17beta-Hydroxyandrost-4-en-3-one 3-phenylpropionate
Testanon 50 (TN)
NSC-26643
DTXCID8028638
Testosterone 17beta-phenpropionate
TESTOSTERONE PHENYL PROPIONATE
Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17-beta)-
TESTOSTERONE PHENYLPROPIONATE [MART.]
TESTOSTERONE PHENYLPROPIONATE [WHO-DD]
3-OXOANDROST-4-EN-17.BETA.-YL 3-PHENYLPROPIONATE
17.BETA.-HYDROXYANDROST-4-EN-3-ONE 3-PHENYLPROPIONATE
TESTOSTERONE PHENYLPROPIONATE (MART.)
Testanon 50
((8R,9S,10R,13S,14S,17S)-10,13-dimethyl-3-oxo-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta(a)phenanthren-17-yl) 3-phenylpropanoate
3-OXOANDROST-4-EN-17BETA-YL 3-PHENYLPROPIONATE
Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17-beta)-(9CI)
hhsxydoroiurip-fezcwrlcsa-n
1255-49-8
Retandrol
Testosterone phenpropionate
Testosterone, hydrocinnamate
Testolent
Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17beta)-
8GN84GWX51
CHEBI:35002
Testosterone 17-Phenylpropionate (1mg/ml in Acetonitrile)
NCGC00160504-01
estosterone phenylpropionate
SCHEMBL940358
GTPL7628
CHEMBL2356993
NSC26643
Tox21_113116
Androst-4-en-3-one, 17-(1-oxo-3-phenylpropoxy)-, (17.beta.)-
AKOS015895428
DS-5641
FD12013
AC-28714
FT177377
CAS-1255-49-8
NS00015426
3-Oxoandrost-4-en-17-yl 3-phenylpropanoate #
D08574
Q27088964
Testosterone 17-phenylpropionate, analytical standard