N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine

Identification

Molecular formula

C₁₇H₁₈ClN

CAS number

63939-13-9

IUPAC name

N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine

State

At room temperature, N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine is typically in a solid state due to its relatively high melting point. However, it can become a viscous liquid if it absorbs some moisture from the environment or is slightly warmed.

Melting point (Celsius)

56.85

Melting point (Kelvin)

330.00

Boiling point (Celsius)

347.40

Boiling point (Kelvin)

620.50

General information

Molecular weight

303.83g/mol

Molar mass

303.8300g/mol

Density

1.1423g/cm³

Appearence

N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine typically appears as a colorless to pale yellow crystalline solid. It may also take a slightly oily form and is usually found in its pure, unadulterated state. The compound is known for its distinct aromatic odor.

Comment on solubility

Solubility of N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine

N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine is a compound that exhibits specific solubility characteristics. Understanding its solubility is crucial for various applications in chemical processes and formulations.

In terms of solubility, we can observe the following:

Polar versus Nonpolar Solvents: This compound is expected to be more soluble in organic solvents due to the nonpolar fluorene structure. Common solvents include ethyl acetate, dichloromethane, and toluene.
Aqueous Solubility: Given the presence of the chloroethyl and amino groups, N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine may have some limited solubility in water, but it is generally not very soluble due to the large hydrophobic fluorene backbone.
Temperature Dependence: Solubility can increase with higher temperatures, particularly in organic solvents. As temperature rises, kinetic energy allows for greater interaction between solute and solvent.
pH Sensitivity: The amino group can undergo protonation in acidic conditions, potentially enhancing solubility in more polar environments, especially under acidic pH.

Overall, the solubility of N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine is a blend of hydrophilic and hydrophobic properties, influencing its use in chemical reactions and formulations. Understanding these aspects allows for better handling and application of this compound in various scientific contexts.

Interesting facts

Interesting Facts about N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine

N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine, often referred to by shorthand in scientific contexts, is a fascinating compound that demonstrates unique properties and applications. This compound belongs to a class of chemical substances known for their potential in various fields, particularly in pharmacology and material science.

Key Characteristics:

Structural Diversity: The compound showcases a distinctive structure that combines elements of fluorenes and amines, which contributes to its chemical reactivity and interactions.
Biological Relevance: It holds potential implications in medicinal chemistry, as compounds containing similar structures have been evaluated for their effects in biological systems.
Chiral Centers: The presence of chiral centers in some analogs can give rise to isomers with differing biological activities, highlighting the importance of stereochemistry in compound synthesis and application.

One interesting aspect of N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine is its role in drug development, where understanding the interactions of such compounds at the molecular level can lead to significant advancements in therapeutic agents. As noted by researchers, “the exploration of structural analogs can illuminate the pathway for new medicinal applications.”

Furthermore, the synthesis of this compound can serve as a model for developing synthetic routes for more complex organic molecules, providing insights that can enhance the fields of both organic synthesis and materials science.

In summary, while N-(2-chloroethyl)-N-ethyl-9H-fluoren-9-amine may not be as widely recognized as some other compounds, its intriguing properties and potential applications make it a worthy subject of study in the expansive field of chemistry.