Skip to main content

Chlorotestosterone acetate

ADVERTISEMENT
Identification
Molecular formula
C25H33ClO6
CAS number
1239-99-8
IUPAC name
[(3S,9S,14S,17R)-17-acetoxy-17-acetyl-6-chloro-10,13-dimethyl-1,2,3,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate
State
State

At room temperature, the compound is typically in a solid state, maintaining a crystalline appearance.

Melting point (Celsius)
198.50
Melting point (Kelvin)
471.65
Boiling point (Celsius)
622.15
Boiling point (Kelvin)
895.15
General information
Molecular weight
456.97g/mol
Molar mass
456.9610g/mol
Density
1.3720g/cm3
Appearence

The compound is typically found in solid form. It is a white to off-white crystalline powder. The structure of the compound suggests a complex polycyclic organization, typical for many steroid derivatives.

Comment on solubility

Solubility of [(3S,9S,14S,17R)-17-acetoxy-17-acetyl-6-chloro-10,13-dimethyl-1,2,3,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate

When discussing the solubility of the compound [(3S,9S,14S,17R)-17-acetoxy-17-acetyl-6-chloro-10,13-dimethyl-1,2,3,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate, several factors need to be considered:

  • Polarity: The presence of functional groups like acetate can influence solubility. Acetate groups tend to enhance solubility in polar solvents.
  • Hydrophobic Regions: The intricate hydrocarbon framework can create hydrophobic interactions, potentially decreasing solubility in water but enhancing it in organic solvents.
  • Solvent Compatibility: This compound is likely to dissolve well in organic solvents such as ethanol, methanol, or DMSO due to its non-polar characteristics.
  • Temperature Effects: Typically, solubility increases with temperature, hence elevated temperatures may assist in dissolving this compound in the appropriate solvent.

In summary, the solubility of [(3S,9S,14S,17R)-17-acetoxy-17-acetyl-6-chloro-10,13-dimethyl-1,2,3,8,9,11,12,14,15,16-decahydrocyclopenta[a]phenanthren-3-yl] acetate is influenced largely by its chemical structure, particularly its balance of polar and non-polar characteristics, which dictates its interactions with various solvents. Understanding these interactions is crucial for applications in both laboratory settings and potential pharmaceutical developments.

Interesting facts

Interesting Facts about the Compound

This unique compound, recognized for its intricate structure and specific stereochemistry, holds significant relevance in the field of organic chemistry and pharmacology. Here are some intriguing aspects:

  • Synthetic Pathways: The synthesis of this compound involves multiple steps of functional group modifications, showcasing the complexities of organic synthesis and the elegance of chemical reactions.
  • Applications in Medicine: Compounds with similar structures are often studied for their potential use as therapeutic agents, particularly in hormonal therapies and cancer treatments.
  • Stereochemistry Matters: The (3S,9S,14S,17R) stereochemistry plays a pivotal role in determining the biological activity of the molecule, influencing how it interacts with biological targets.
  • Drug Development: The exploration of such compounds contributes to the design of novel drugs that can effectively target specific receptors or pathways in the body, opening doors to new treatment options.
  • Natural Analogues: Many synthetic compounds are inspired by natural products; understanding the structure and function of this compound can help in the development of synthetic analogues with improved efficacy.

As researchers delve deeper into the properties and reactions of this compound, it can lead to discoveries that not only enhance our understanding of organic chemistry but also contribute to advancements in healthcare and pharmaceuticals.

In the words of a noted chemist, "Every compound has a story to tell; understanding its narrative can lead to groundbreaking innovations."