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Allylestrenol

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Identification
Molecular formula
C21H32O2
CAS number
432-60-0
IUPAC name
17-allyl-17-hydroxy-13-methyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
State
State

At room temperature, Allylestrenol is in a solid state as a white crystalline powder.

Melting point (Celsius)
119.12
Melting point (Kelvin)
392.30
Boiling point (Celsius)
380.15
Boiling point (Kelvin)
653.30
General information
Molecular weight
310.48g/mol
Molar mass
310.4750g/mol
Density
1.0611g/cm3
Appearence

Allylestrenol appears as a white crystalline powder. It is odourless and relatively stable under normal conditions.

Comment on solubility

Solubility Overview

The solubility of 17-allyl-17-hydroxy-13-methyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one, a complex organic compound, is influenced by various factors related to its chemical structure and interactions with solvents.

Factors Affecting Solubility

Key factors determining the solubility of this compound include:

  • Molecular Structure: The presence of multiple hydroxy groups can enhance solubility in polar solvents.
  • Polarity: The overall polarity of the molecule dictates its compatibility with solvent types.
  • Hydrophobic Interactions: Alkyl substituents may contribute to hydrophobic behavior, affecting solubility in aqueous environments.
  • Temperature: Solubility generally increases with temperature, enabling better interactions in various solvents.

Solvent Compatibility

When considering possible solvents, one might categorize them as follows:

  • Polar Solvents: Such as methanol and ethanol, likely to dissolve the compound due to the presence of hydroxyl groups.
  • Non-Polar Solvents: Like hexane or toluene, might show limited solubility due to the hydrophobic nature of certain structural components.

In summary, the solubility of this compound is complex and variable. As noted, "solubility is governed by the principle of 'like dissolves like'," meaning that the chemical characteristics of both the solute and solvent are crucial for determining how well they interact. Therefore, comprehensive experimental data would be invaluable for precise solubility assessments in various solvents.

Interesting facts

Interesting Facts about 17-allyl-17-hydroxy-13-methyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one

This compound, often scrutinized within the realm of steroid chemistry, holds intriguing potential due to its structural configuration. Here are some noteworthy points about this chemical compound:

  • Structural Complexity: With its unique octahydrocyclopenta[a]phenanthrene framework, this compound showcases a fascinating blend of saturated and aromatic characteristics, leading to interesting stereochemistry.
  • Biological Activity: It is believed to modulate various biological pathways, which opens doors for research in medicinal chemistry and pharmacology. This compound has attracted interest for potential therapeutic implications in hormone-related therapies.
  • Synthetic Pathways: The synthesis of such complex molecules usually requires multi-step reactions involving intricate methodologies, showcasing the creativity and resourcefulness of synthetic chemists.
  • Research Potential: As newer biological assays and screens are developed, compounds like this one can be pivotal in drug discovery processes aimed at hormone regulation.
  • Derivative Importance: Modifications to the base structure may lead to derivatives with enhanced biological activity, demonstrating the versatility of steroid analogs in chemical research.

In summary, the study of 17-allyl-17-hydroxy-13-methyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one is rich in possibilities. As researchers continue to explore its landscape, there is much anticipation for its contributions to chemistry and medicine.

Synonyms
(17R)-17-Hydroxy-13-methyl-17-prop-2-enyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
NCGC00183119-01
SCHEMBL3875096
CHEMBL2138313
DTXSID30859548
CHEBI:230024
AKOS015896699
17-hydroxy-13-methyl-17-prop-2-enyl-1,2,6,7,8,14,15,16-octahydrocyclopenta[a]phenanthren-3-one
DB-056845
17-Hydroxy-13-methyl-17-(prop-2-en-1-yl)-1,2,6,7,8,13,14,15,16,17-decahydro-3H-cyclopenta[a]phenanthren-3-one