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6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b]benzofuran-1,8b-diol

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Identification
Molecular formula
C28H24O6
CAS number
135105-53-6
IUPAC name
6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b]benzofuran-1,8b-diol
State
State
At room temperature, the compound is likely a solid, considering its complex structure and relatively high molar mass.
Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
440.49g/mol
Molar mass
440.4890g/mol
Density
0.0000g/cm3
Appearence
.
Comment on solubility

Solubility of 6,8-Dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b]benzofuran-1,8b-diol

The compound 6,8-dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b]benzofuran-1,8b-diol, represented by the chemical formula C28H24O6, exhibits notable characteristics regarding its solubility. Here are some key points to consider:

  • Solvent Type: This compound is likely to be soluble in polar organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO), which can facilitate the dissolution of the molecule due to its polar functional groups.
  • Hydrophobic Interactions: The hydrophobic regions contributed by the phenyl and methoxy groups may hinder solubility in water, indicating limited aqueous solubility.
  • Temperature Influence: As with many organic compounds, solubility can increase with temperature, allowing for greater solubility in organic solvents as the kinetic energy of the molecules increases.
  • Chemical Nature: The presence of multiple methoxy groups may contribute to the compound's overall solubility profile, as methoxy groups can help to stabilize the compound in a solvent through dipole interactions.

In conclusion, while the compound is anticipated to be soluble in various organic solvents due to its functional groups, its solubility in water is likely to be low. Careful consideration of solvent selection is crucial for optimal dissolution.

Interesting facts

Exploring 6,8-Dimethoxy-3a-(4-methoxyphenyl)-3-phenyl-2,3-dihydro-1H-cyclopenta[b]benzofuran-1,8b-diol

This fascinating compound, often referred to as a member of the cyclopenta[b]benzofuran family, showcases a range of intriguing characteristics that make it a subject of interest in both synthetic and natural product chemistry.

Key Features of the Compound:

  • Structural Complexity: The presence of multiple rings and functional groups contributes to its intricate structure, which can be a challenge and a delight for chemists working on synthesis.
  • Potential Biological Activity: Compounds like this often exhibit promising pharmacological properties, making them candidates for drug development. Research into similar structures has indicated various biological activities, including anticancer and antioxidant effects.
  • Natural Origins: Many compounds of this type are isolated from plants and fungi, which highlights the importance of biodiversity in medicinal chemistry. Understanding how these compounds are synthesized in nature can inspire new synthetic methods.
  • Versatile Functional Groups: The presence of methoxy groups suggests electron-donating effects, which can influence the compound's reactivity and interactions with biological systems.

Research Insights:

As researchers delve deeper into the pharmacological potential of such compounds, it's essential to consider:

  1. The importance of structure-activity relationships (SAR) in discovering new therapeutic agents.
  2. How variations in substitution patterns can lead to different biological profiles.
  3. The role of synthetic routes in developing more efficient and environmentally friendly methods of production.

Understanding cyclopenta[b]benzofurans like this compound can pave the way for breakthroughs in medicinal chemistry, showcasing the beauty and complexity of chemical synthesis and its applications in health sciences.

Synonyms
Ferrugin
SCHEMBL6323415
AKOS032948596
PD129720