9-(m-tolyl)fluorene | Solubility of Things

Identification

Molecular formula

C₂₀H₁₆

CAS number

161589-16-2

IUPAC name

9-(m-tolyl)-9H-fluorene

State

At room temperature, 9-(m-tolyl)fluorene is found in a solid state. Its stability in this state makes it suitable for various chemical and industrial applications.

Melting point (Celsius)

128.40

Melting point (Kelvin)

401.55

Boiling point (Celsius)

454.50

Boiling point (Kelvin)

727.65

General information

Molecular weight

254.35g/mol

Molar mass

254.3300g/mol

Density

1.1454g/cm³

Appearence

9-(m-Tolyl)fluorene is a solid compound that typically appears as white to off-white crystalline powder. Its crystalline form enables it to be used effectively in various applications, particularly those that require precise color characteristics.

Comment on solubility

Solubility of 9-(m-tolyl)-9H-fluorene

9-(m-tolyl)-9H-fluorene is a compound whose solubility can vary significantly based on environmental factors. Here are some key points regarding its solubility:

Solvent Dependence: The solubility of 9-(m-tolyl)-9H-fluorene is primarily influenced by the choice of solvent. It tends to be more soluble in organic solvents such as toluene and benzene due to its hydrophobic characteristics.
Temperature Effects: Like many organic compounds, its solubility can increase with temperature. Higher temperatures often lead to improved solvation and dissolving efficiency.
Hydrophobic Interactions: The presence of aromatic rings contributes to its low solubility in polar solvents like water. This results from hydrophobic interactions, which hinder its entrapment in polar solvent matrices.

In summary, 9-(m-tolyl)-9H-fluorene exhibits variable solubility primarily governed by solvent choice, temperature, and molecular interactions. Understanding these factors is essential for its effective application in various chemical processes.

Interesting facts

Interesting Facts About 9-(m-tolyl)-9H-fluorene

9-(m-tolyl)-9H-fluorene is an intriguing compound that has garnered attention in various fields of chemistry, particularly in organic synthesis and materials science. Here are some fascinating aspects of this compound:

Structural Characteristics: This compound features a unique combination of a fluorene backbone with a m-tolyl group. This results in interesting electronic and photophysical properties, making it a subject of study for those exploring new organic materials.

Applications in Organic Electronics: Due to its luminescent properties, 9-(m-tolyl)-9H-fluorene is potentially applicable in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics. These applications are crucial for creating more efficient and flexible electronic devices.

Research Significance: The compound serves as a building block in the synthesis of more complex organic materials. Chemists often use derivatives of fluorene to explore new chemical reactions and to develop novel materials with tailored properties.

Chemical Behavior: Understanding the reactivity of 9-(m-tolyl)-9H-fluorene can offer insights into the behavior of similar compounds. This can help predict outcomes in reactions involving aromatic compounds and provide a deeper understanding of aromaticity.

Versatile Functionalization: The presence of multiple substitution sites on the fluorene ring allows for versatile functionalization of this compound, enabling researchers to customize its properties for specific applications, from pharmaceuticals to materials science.

In summary, 9-(m-tolyl)-9H-fluorene exemplifies the beauty of organic chemistry through its structural complexity and potential applications. As researchers continue to explore its properties and behavior, it may lead to groundbreaking advancements in technology and materials science.

Synonyms

9-(3-METHYLPHENYL)-9H-FLUORENE

18153-42-9

DTXSID40171162

DTXCID8093653

9-m-tolylfluorene

SCHEMBL28038360

SCHEMBL28946044