8,9,10,11-tetrahydrobenzo[b]phenanthrene-8,9,10-triol

Identification

Molecular formula

C₁₇H₁₆O₃

CAS number

54556-98-8

IUPAC name

8,9,10,11-tetrahydrobenzo[b]phenanthrene-8,9,10-triol

State

This compound is in a solid state at room temperature.

Melting point (Celsius)

230.00

Melting point (Kelvin)

503.15

Boiling point (Celsius)

407.00

Boiling point (Kelvin)

680.15

General information

Molecular weight

274.32g/mol

Molar mass

274.3180g/mol

Density

1.2500g/cm³

Appearence

The compound is typically solid at room temperature, appearing as a white to off-white crystalline powder. Its appearance may depend on the specific conditions like purity and the presence of any polymorphic forms.

Comment on solubility

Solubility of 8,9,10,11-tetrahydrobenzo[b]phenanthrene-8,9,10-triol

The solubility of 8,9,10,11-tetrahydrobenzo[b]phenanthrene-8,9,10-triol (C₁₇H₁₆O₃) is an intriguing topic due to its unique structural characteristics. As a polycyclic compound with multiple hydroxyl groups, its solubility properties can vary significantly depending on the solvent medium. Here are some key points to consider:

Water Solubility: The presence of three hydroxyl (–OH) groups suggests potential for hydrogen bonding with water molecules; however, the overall hydrophobic character contributed by the polycyclic structure may limit its solubility in aqueous solutions.
Organic Solvent Solubility: This compound is likely to be more soluble in organic solvents such as ethanol, methanol, or dichloromethane, which can effectively disrupt the hydrophobic interactions and allow solvation.
Hydrogen Bonding: The ability to form hydrogen bonds due to the hydroxyl groups enhances solubility in polar solvents, making it more likely to dissolve in environments that can accommodate such interactions.

In conclusion, while 8,9,10,11-tetrahydrobenzo[b]phenanthrene-8,9,10-triol may not exhibit high solubility in water, it will show increased solubility in polar organic solvents. As with many compounds, the interplay between its hydrophobic and hydrophilic features fundamentally dictates its solubility behavior in various solvents.

Interesting facts

Interesting Facts about 8,9,10,11-Tetrahydrobenzo[b]phenanthrene-8,9,10-triol

8,9,10,11-tetrahydrobenzo[b]phenanthrene-8,9,10-triol, often referred to in research as a *hydroxylated polycyclic aromatic hydrocarbon*, is a compound that presents intriguing features worthy of exploration:

Polycyclic Structure: This compound contains a complex arrangement of fused rings, making it fascinating for studies in organic chemistry and materials science.
Biologically Active Metabolite: As a triol, it possesses functional hydroxyl groups that may influence biological activity and interact with various biological systems.
Potential Applications: Research has indicated that derivatives of this compound may have applications in drug development, especially in the fields of cancer therapy and environmental science, as it can serve as a marker for pollution studies.
Environmental Relevance: Understanding compounds like this one is vital in assessing the impacts of polycyclic aromatic hydrocarbons (PAHs) on human health and the environment.
Research Interest: The compound is subject to ongoing studies in various fields due to its complex structure and potential for reactivity, making it a valuable topic in advanced organic synthesis.

As a chemistry student or a researcher, exploring this compound can provide insights into both its chemical properties and practical implications in science, enriching the understanding of how complex organic molecules function.

Synonyms

Benz[a]anthracene-8,9,10-triol, 8,9,10,11-tetrahydro-

89458-22-0

DTXSID60274341